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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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Published in: | Frontiers in genetics 2018, Vol.9, p.110-110 |
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Format: | Report |
Language: | English |
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container_end_page | 110 |
container_issue | |
container_start_page | 110 |
container_title | Frontiers in genetics |
container_volume | 9 |
creator | Tsai, Meng-Che Yu, Hui-Wen Liu, Tsunglin Chou, Yen-Yin Chiou, Yuan-Yow Chen, Peng-Chieh |
description | |
doi_str_mv | 10.3389/fgene.2018.00110 |
format | report |
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ispartof | Frontiers in genetics, 2018, Vol.9, p.110-110 |
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language | eng |
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source | PubMed Central |
title | Rare Compound Heterozygous Frameshift Mutations in ALMS1 Gene Identified Through Exome Sequencing in a Taiwanese Patient With Alström Syndrome |
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