(Q36403852)

14 August 2017

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. (English)

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hypertrophic cardiomyopathy

14 August 2017

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familial hypertrophic cardiomyopathy

inferred from title

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inferred from title

author

Hugh Christian Watkins

3

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14 August 2017

10

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14 August 2017

L Thierfelder

1

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14 August 2017

C MacRae

2

1 reference

14 August 2017

J Tomfohrde

4

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14 August 2017

M Williams

5

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14 August 2017

W McKenna

6

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14 August 2017

K Bohm

7

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14 August 2017

G Noeske

8

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14 August 2017

M Schlepper

9

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14 August 2017

language of work or name

English

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publication date

1 July 1993

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Proceedings of the National Academy of Sciences of the United States of America

14 August 2017

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14 August 2017

90

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14 August 2017

13

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14 August 2017

6270-6274

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A molecular basis for familial hypertrophic cardiomyopathy: an alpha/beta cardiac myosin heavy chain hybrid gene

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the beta-myosin heavy chain gene. A 908Leu----Val mutation and a 403Arg----Gln mutation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

The gene responsible for familial hypocalciuric hypercalcemia maps to chromosome 3q in four unrelated families

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

A computer program for linkage analysis of general human pedigrees

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=46910

Patterns and significance of distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy. A wide angle, two dimensional echocardiographic study of 125 patients

28 June 2018

1 reference

12 December 2020

Distribution of left ventricular hypertrophy in hypertrophic cardiomyopathy: a two-dimensional echocardiographic study

1 reference

12 December 2020

Echocardiographic measurement of right ventricular wall thickness in hypertrophic cardiomyopathy: relation to clinical and prognostic features

1 reference

12 December 2020

Mapping a gene for familial hypertrophic cardiomyopathy to chromosome 14q1

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12 December 2020

Identifiers

DOI

10.1073/PNAS.90.13.6270

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14 August 2017

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14 August 2017

PubMed publication ID

8327508

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