PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

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Correction of Monogenic and Common Retinal Disorders with Gene Therapy.Phenotypic expansion and progression of SPATA7-associated retinitis pigmentosa.CHOROIDEREMIA ASSOCIATED WITH A NOVEL SYNONYMOUS MUTATION IN GENE ENCODING REP-1.

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PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

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http://www.wikidata.org/entity/Q53033713

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

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2017年学术文章

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2017年學術文章

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name

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

@en

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

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type

Item

label

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

@en

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

@nl

prefLabel

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

@en

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

@nl

P1476

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

@en

P2093

James Lin

http://www.w3.org/2001/XMLSchema#string

Katherine Boudreault

http://www.w3.org/2001/XMLSchema#string

Kevin K Ma

http://www.w3.org/2001/XMLSchema#string

Royce W S Chen

http://www.w3.org/2001/XMLSchema#string

Stephen H Tsang

http://www.w3.org/2001/XMLSchema#string

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Evaluation of retinal photoreceptors and pigment epithelium in a female carrier of choroideremia

Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene.

Quantitative optical coherence tomography angiography of vascular abnormalities in the living human eye

Choroideremia: a review of general findings and pathogenesis.

Progression of retinal pigment epithelial alterations during long-term follow-up in female carriers of choroideremia and report of a novel CHM mutation.

Detection of mosaic retinal dysfunction in choroideremia carriers electroretinographic and psychophysical testing.

Choroideremia: variability of clinical and electrophysiological characteristics and first report of a negative electroretinogram.

Remodeling of the Human Retina in Choroideremia: Rab Escort Protein 1 (REP-1) Mutations

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scholarly article

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10.1097/ICB.0000000000000419

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11 Suppl 1

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2017-12-01T00:00:00Z

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27599108

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PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

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P2860

P2860

PHENOTYPING CHOROIDEREMIA AND ITS CARRIER STATE WITH MULTIMODAL IMAGING TECHNIQUES.

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P1433

P1476

P2093

P2860

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P356

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P577

P698

P932

P356

P1433

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P2860

P304

P31

P356

P478

P577

P698

P932