Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa

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Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosa

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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Characterization of macular st ...... dominant retinitis pigmentosa

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Characterization of macular st ...... dominant retinitis pigmentosa

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Characterization of macular st ...... dominant retinitis pigmentosa

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P1476

Characterization of macular st ...... dominant retinitis pigmentosa

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P2093

Sten Andréasson

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Ulrika Kjellström

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Vesna Ponjavic

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Wissam Abdulridha-Aboud

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P2860

Retinitis pigmentosa

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Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa

In diabetic retinopathy, foveal thickness of 300 mum seems to correlate with functionally significant loss of vision.

Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports.

Macular abnormalities in Italian patients with retinitis pigmentosa.

Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern Sweden.

A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).

A novel recessive GUCY2D mutation causing cone-rod dystrophy and not Leber's congenital amaurosis

Genes and mutations causing retinitis pigmentosa.

P304

362-373

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P31

scholarly article

P478

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P577

2016-05-22T00:00:00Z

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P698

27212874

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P932

4860447

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