An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness (Q24315182)

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13 November 2019

title

An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness (English)

1 reference

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congenital stationary night blindness

13 November 2019

main subject

congenital disorder

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Calcium voltage-gated channel subunit alpha1 F

1 reference

GOA release 2020-03-11

visual perception

1 reference

X-linked congenital stationary night blindness

GOA release 2020-03-11

1 reference

6

1 reference

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13 November 2019

Eberhart Zrenner

12

1 reference

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13 November 2019

Thomas Meitinger

13

1 reference

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15

Meindl A

1 reference

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13 November 2019

Eckart Apfelstedt-Sylla

3

object named as

Apfelstedt-Sylla E

1 reference

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13 November 2019

author name string

Strom TM

1

1 reference

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13 November 2019

Nyakatura G

2

1 reference

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13 November 2019

Hellebrand H

4

1 reference

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13 November 2019

Lorenz B

5

1 reference

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13 November 2019

Wutz K

7

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13 November 2019

Gutwillinger N

8

1 reference

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13 November 2019

Rüther K

9

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13 November 2019

Drescher B

10

1 reference

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13 November 2019

Sauer C

11

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13 November 2019

Rosenthal A

14

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13 November 2019

language of work or name

English

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publication date

1 July 1998

1 reference

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13 November 2019

1 reference

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13 November 2019

volume

19

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13 November 2019

issue

3

1 reference

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page(s)

260-263

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[Analysis of the human electroretinogram]

13 November 2019

cites work

1 reference

7 January 2021

Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus

1 reference

7 January 2021

Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region

1 reference

7 January 2021

Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.

1 reference

7 January 2021

Models of the normal and abnormal rod system

1 reference

7 January 2021

Dependence of photoreceptor glutamate release on a dihydropyridine-sensitive calcium channel

1 reference

7 January 2021

Cloning of the human skeletal muscle alpha 1 subunit of the dihydropyridine-sensitive L-type calcium channel (CACNL1A3)

1 reference

7 January 2021

Cloning, chromosomal localization, and functional expression of the alpha 1 subunit of the L-type voltage-dependent calcium channel from normal human heart

1 reference

7 January 2021

Structure and functional expression of alpha 1, alpha 2, and beta subunits of a novel human neuronal calcium channel subtype

1 reference

7 January 2021

Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp

1 reference

7 January 2021

Prediction of complete gene structures in human genomic DNA

1 reference

7 January 2021

Locating protein-coding regions in human DNA sequences by a multiple sensor-neural network approach

1 reference

7 January 2021

Structural parts involved in activation and inactivation of the sodium channel

1 reference

7 January 2021

The IVS6 segment of the L-type calcium channel is critical for the action of dihydropyridines and phenylalkylamines.

1 reference

7 January 2021

Nine L-type amino acid residues confer full 1,4-dihydropyridine sensitivity to the neuronal calcium channel alpha1A subunit. Role of L-type Met1188.

1 reference

7 January 2021

Calcium channel β-subunit binds to a conserved motif in the I–II cytoplasmic linker of the α1-subunit

1 reference

7 January 2021

Gain of rod to horizontal cell synaptic transfer: relation to glutamate release and a dihydropyridine-sensitive calcium current

1 reference

7 January 2021

B-wave of the electroretinogram. A reflection of ON bipolar cell activity

1 reference

7 January 2021

Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval

1 reference

7 January 2021

A new DNA sequence assembly program

1 reference

7 January 2021

Developmental expression patterns of mouse sFRP genes encoding members of the secreted frizzled related protein family.

1 reference

7 January 2021

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

1 reference

7 January 2021

Identifiers

DOI

10.1038/940

2 references

Consolidated OpenCitations Corpus – April 2017

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Dimensions Publication ID

13 November 2019

1024671199

0 references

1 reference

Consolidated OpenCitations Corpus – April 2017

2 references

Consolidated OpenCitations Corpus – April 2017