Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy.

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Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy.

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

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2016年论文

@zh

2016年论文

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Novel OPN1LW/OPN1MW deletion m ...... s with blue cone monochromacy.

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Novel OPN1LW/OPN1MW deletion m ...... s with blue cone monochromacy.

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Novel OPN1LW/OPN1MW deletion m ...... s with blue cone monochromacy.

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P1476

Novel OPN1LW/OPN1MW deletion mutations in 2 Japanese families with blue cone monochromacy

@en

P2093

Chunxia Wang

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Hiroko Terasaki

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Katsuhiro Hosono

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Kimiko Suto

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Makoto Nakamura

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Shinsei Minoshima

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Shu Kachi

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Yozo Miyake

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P2860

Molecular genetics of human color vision: the genes encoding blue, green, and red pigments

Genetic heterogeneity among blue-cone monochromats

Molecular genetics of inherited variation in human color vision

Bilateral macular atrophy in blue cone monochromacy (BCM) with loss of the locus control region (LCR) and part of the red pigment gene.

Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy.

Blue cone monochromacy: causative mutations and associated phenotypes.

A locus control region adjacent to the human red and green visual pigment genes.

Molecular genetics of human blue cone monochromacy.

High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy

Novel RDH5 mutation in family with mother having fundus albipunctatus and three children with retinitis pigmentosa.

P2888

hgv.2016.11

P304

16011

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P31

scholarly article

P356

10.1038/HGV.2016.11

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P478

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P50

Yoshihiro Hotta

P577

2016-05-26T00:00:00Z

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P698

27274860

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P932

4880642

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