(Q28143893)

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A novel compound heterozygous mutation in the RDH5 gene in a patient with fundus albipunctatus

scientific article (publication date: November 2000)

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A novel compound heterozygous mutation in the RDH5 gene in a patient with fundus albipunctatus (English)

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S Kuroiwa

1

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T Kikuchi

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2

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N Yoshimura

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3

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language of work or name

English

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publication date

November 2000

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published in

American Journal of Ophthalmology

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volume

130

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issue

5

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page(s)

672-5

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cites work

Fundus albipunctatus associated with cone dystrophy

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https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900765-0

retrieved

7 January 2021

Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus

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https://api.crossref.org/works/10.1016%2FS0002-9394%2800%2900765-0

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7 January 2021

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DOI

10.1016/S0002-9394(00)00765-0

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PubMed ID

11078852

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(Q28143893)

A novel compound heterozygous mutation in the RDH5 gene in a patient with fundus albipunctatus

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