Whole exome sequencing identified two homozygous ALMS1 mutations in an Iranian family with Alström syndrome 22 June 2020 | 09:40 Code : 10016 New Features Send To Others Your Name Your Email Recipient Email Send Cancel visits:20825 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
