Whole exome sequencing in thai patients with retinitis pigmentosa reveals novel mutations in six genes

Whole exome sequencing in thai patients with retinitis pigmentosa reveals novel mutations in six genes

Purpose. To identify disease-causing mutations and describe genotype-phenotype correlations in Thai patients with nonsyndromic retinitis pigmentosa (RP). Methods. Whole exome sequencing was performed in 20 unrelated patients. Eighty-six genes associated with RP, Leber congenital amaurosis, and cone-...

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Main Authors: Worapoj Jinda, Todd D. Taylor, Yutaka Suzuki, Wanna Thongnoppakhun, Chanin Limwongse, Patcharee Lertrit, Prapat Suriyaphol, Adisak Trinavarat, La Ongsri Atchaneeyasakul
Other Authors: Mahidol University
Format: Article
Published: 2018
Subjects:
Medicine
Neuroscience
Online Access:https://repository.li.mahidol.ac.th/handle/123456789/34253
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Institution: Mahidol University

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https://repository.li.mahidol.ac.th/handle/123456789/34253

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