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Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome

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Bibliographic Details
Published in:Frontiers in genetics 2018, Vol.9, p.110-110
Main Authors: Tsai, Meng-Che, Yu, Hui-Wen, Liu, Tsunglin, Chou, Yen-Yin, Chiou, Yuan-Yow, Chen, Peng-Chieh
Format: Report
Language:English
Online Access:Get full text
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ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2018.00110