Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis. (Q41108843)

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17 February 2020

title

Novel GUCY2D Gene Mutations in Japanese Male Twins with Leber Congenital Amaurosis (English)

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17 February 2020

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7

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17 February 2020

author name string

Katsuhiro Hosono

1

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17 February 2020

Yuko Harada

2

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17 February 2020

Kentaro Kurata

3

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17 February 2020

Akiko Hikoya

4

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17 February 2020

Miho Sato

5

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17 February 2020

Shinsei Minoshima

6

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17 February 2020

publication date

13 May 2015

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17 February 2020

published in

Journal of Ophthalmology

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17 February 2020

volume

2015

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17 February 2020

page(s)

693468

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Creative Commons Attribution 3.0 Unported

17 February 2020

copyright license

start time

1 January 2015

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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April 2022 Public Data File from Crossref

copyrighted

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Mutations that are a common cause of Leber congenital amaurosis in northern America are rare in southern India

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12 December 2020

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Identifiers

DOI

10.1155/2015/693468

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26097748%20AND%20SRC:MED&resulttype=core&format=json

17 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26097748%20AND%20SRC:MED&resulttype=core&format=json

17 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:26097748%20AND%20SRC:MED&resulttype=core&format=json