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Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome

22 June 2020 | 09:40 Code : 10016 New Features

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http://https://www.ncbi.nlm.nih.gov/pubmed/31560378

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6797882/

http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2019;volum...