COL4A1 mutations cause ocular dysgenesis, neuronal localization defects, and myopathy in mice and Walker-Warburg syndrome in humans (Q28478186)

9

object named as

Christopher A Walsh

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author name string

Cassandre Labelle-Dumais

1

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David J Dilworth

2

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Emily P Harrington

3

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Michelle de Leau

4

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David Lyons

5

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Zhyldyz Kabaeva

6

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M Chiara Manzini

7

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Daniel E Michele

10

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Douglas B Gould

Creative Commons Attribution 4.0 International

11

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language of work or name

English

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publication date

May 2011

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published in

PLOS Genetics

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volume

7

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issue

5

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page(s)

e1002062

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copyright license

start time

19 May 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Parental mosaicism and autosomal dominant mutations causing structural abnormalities of collagen I are frequent in families with osteogenesis imperfecta type III/IV

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