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

01 June 2020 | 11:02 Code : 9698 New Features

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https://www.ncbi.nlm.nih.gov/pubmed/?term=Whole+Exome+Sequencing+identified+two+homozygous+ALMS1+Mutations+in+an+Iranian+Family+with+Alstr%C3%B6m+Syndrome

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