Investigation of SLA4A3 as a candidate gene for human retinal disease

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Investigation of SLA4A3 as a candidate gene for human retinal disease

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2016 nî lūn-bûn

@nan

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

@wuu

2016年论文

@zh

2016年论文

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Investigation of SLA4A3 as a candidate gene for human retinal disease

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Investigation of SLA4A3 as a candidate gene for human retinal disease

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Investigation of SLA4A3 as a candidate gene for human retinal disease

@en

P1476

Investigation of SLA4A3 as a candidate gene for human retinal disease

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P2093

Andrew R Webster

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Anthony T Moore

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Cathryn S Mellersh

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Louise M Downs

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Michel Michaelides

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Robin R Ali

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P2860

A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations

Mutations in RPE65 cause autosomal recessive childhood-onset severe retinal dystrophy

Molecular cloning, expression, and chromosomal localization of two isoforms of the AE3 anion exchanger from human heart

Mice with a targeted disruption of the Cl-/HCO3- exchanger AE3 display a reduced seizure threshold

Molecular physiology and genetics of Na+-independent SLC4 anion exchangers

Mutations in the RPE65 gene in patients with autosomal recessive retinitis pigmentosa or leber congenital amaurosis

A method and server for predicting damaging missense mutations

Primer3 on the WWW for general users and for biologist programmers

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

Regulation of intracellular pH by a neuronal homolog of the erythrocyte anion exchanger

P304

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P31

scholarly article

case report

P356

10.1186/S12952-016-0054-Z

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P478

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P50

Alison J Hardcastle

P577

2016-05-23T00:00:00Z

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P698

27211793

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P932

4876561

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