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Exome sequencing in families with chronic central serous chorioretinopathy

BACKGROUND: Central serous chorioretinopathy (CSC) is a chorioretinal disease characterized by fluid accumulation between the neuroretina and retinal pigment epithelium with unknown etiology. Family studies have suggested a heritable component for CSC with an autosomal dominant inheritance pattern....

詳細記述

保存先:
書誌詳細
出版年:Mol Genet Genomic Med
主要な著者: Schellevis, Rosa L., van Dijk, Elon H. C., Breukink, Myrte B., Keunen, Jan E. E., Santen, Gijs W. E., Hoyng, Carel B., de Jong, Eiko K., Boon, Camiel J. F., den Hollander, Anneke I.
フォーマット: Artigo
言語:Inglês
出版事項: John Wiley and Sons Inc. 2019
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6465660/
https://ncbi.nlm.nih.gov/pubmed/30724488
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.576
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