Simultaneous Presence of Macular Corneal Dystrophy and Retinitis Pigmentosa in Three Members of a Family.

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Simultaneous Presence of Macular Corneal Dystrophy and Retinitis Pigmentosa in Three Members of a Family.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Simultaneous Presence of Macul ...... in Three Members of a Family.

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Simultaneous Presence of Macul ...... in Three Members of a Family.

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Item

label

Simultaneous Presence of Macul ...... in Three Members of a Family.

@en

Simultaneous Presence of Macul ...... in Three Members of a Family.

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prefLabel

Simultaneous Presence of Macul ...... in Three Members of a Family.

@en

Simultaneous Presence of Macul ...... in Three Members of a Family.

@nl

P1476

Simultaneous Presence of Macul ...... in Three Members of a Family.

@en

P2093

Farhad Nejat

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Hossein Aghamollaei

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Khosrow Jadidi

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Mohammad Amin Nejat

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Shiva Pirhadi

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P2860

RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy

Linkage of a gene for macular corneal dystrophy to chromosome 16

Retinitis pigmentosa

Advances in the molecular genetics of corneal dystrophies.

CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic review.

Pathophysiology of Corneal Dystrophies: From Cellular Genetic Alteration to Clinical Findings.

SPATA7: Evolving phenotype from cone-rod dystrophy to retinitis pigmentosa

Clinical findings and common symptoms in retinitis pigmentosa.

Retinitis pigmentosa and granular dystrophy: a rare and unique combination in one patient.

Novel mutations in the carbohydrate sulfotransferase gene (CHST6) in American patients with macular corneal dystrophy.

P304

227-230

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P31

scholarly article

case report

P433

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P478

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P577

2018-03-01T00:00:00Z

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P698

29749994

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P932

5936857

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