Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

New Research: Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families: Background: Alström syndrome (AS) is a very rare childhood disorder characterized by… https://t.co/94D9Y1Gf4S #Pe