Exome sequencing in families with chronic central serous chorioretinopathy.

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作者： Rosa L,Schellevis ^[1] ; Elon H C,van Dijk ^[2] ; Myrte B,Breukink ^[1] ; Jan E E,Keunen ^[1] ; Gijs W E,Santen ^[3] ; Carel B,Hoyng ^[1] ; Eiko K,de Jong ^[1] ; Camiel J F,Boon ^[2] ; Anneke I,den Hollander ^[4]

作者单位： Department of Ophthalmology, Donders Institute of Brain, Cognition, and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands. ^[1] Department of Ophthalmology, Leiden University Medical Center, Leiden, The Netherlands. ^[2] Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands. ^[3] Department of Ophthalmology, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, The Netherlands. ^[4] Department of Human Genetics, Donders Institute of Brain, Cognition, and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands. ^[5]

关键词 PTPRB RareIBD chronic central serous chorioretinopathy exome sequencing families

主题词中心性浆液性脉络膜视网膜病变(Central Serous Chorioretinopathy);女(雌)性(Female);基因频率(Gene Frequency);人类(Humans);男(雄)性(Male);系谱(Pedigree);受体样蛋白质酪氨酸磷酸酶类, 3类(Receptor-Like Protein Tyrosine Phosphatases, Class 3)

DOI 10.1002/mgg3.576

PMID 30724488

发布时间 2022-12-07

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Molecular genetics & genomic medicine

2019年7卷4期

e00576页

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Exome sequencing in families with chronic central serous chorioretinopathy.

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

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Exome sequencing in families with chronic central serous chorioretinopathy.

Molecular genetics & genomic medicine

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Molecular genetics & genomic medicine

相关期刊

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