Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome 01 June 2020 | 11:02 Code : 9698 New Features Send To Others Your Name Your Email Recipient Email Send Cancel visits:19859 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
