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Molecular genetic characteristics of X-linked retinoschisis in Koreans

PURPOSE: X-linked retinoschisis (XLRS) is a recessively inherited disorder that causes macular degeneration and resultant visual defect in young males. Many genetic studies had focused on the patients in Western countries. We characterized the mutational spectrum of the RS1 gene in Korean patients w...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Kim, So Yeon, Ko, Hyun Soo, Yu, Young Suk, Hwang, Jeong-Min, Lee, Jong Joo, Kim, Sung Yeun, Kim, Ji Yeon, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Molecular Vision 2009
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2672147/
https://ncbi.nlm.nih.gov/pubmed/19390641
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