Open AccessWhole exome sequencing identified novel homozygous ALMS1 variant in a Tunisian family with Alström syndrome
Author(s) -
Imen Habibi
Publication year - 2019
Publication title -
annals of case reports
Language(s) - English
Resource type - Journals
ISSN - 2574-7754
DOI - 10.29011/2574-7754/100379
Subject(s) - exome sequencing , exome , genetics , computational biology , dna sequencing , biology , gene , mutation