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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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Main Authors: | , , , , , |
Format: | Report |
Language: | English |
Online Access: | Get full text |
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Summary: | |
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ISSN: | 1664-8021 1664-8021 |
DOI: | 10.3389/fgene.2018.00110 |