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Application of Whole Exome and Targeted Panel Sequencing in the Clinical Molecular Diagnosis of 319 Chinese Families with Inherited Retinal Dystrophy and Comparison Study

Inherited retinal dystrophies (IRDs) are a group of clinically and genetically heterogeneous diseases involving more than 280 genes and no less than 20 different clinical phenotypes. In this study, our aims were to identify the disease-causing gene variants of 319 Chinese patients with IRD, and comp...

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Dettagli Bibliografici
Pubblicato in:Genes (Basel)
Autori principali: Wang, Likun, Zhang, Jinlu, Chen, Ningning, Wang, Lei, Zhang, Fengsheng, Ma, Zhizhong, Li, Genlin, Yang, Liping
Natura: Artigo
Lingua:Inglês
Pubblicazione: MDPI 2018
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6071067/
https://ncbi.nlm.nih.gov/pubmed/30029497
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes9070360
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