Publications
Export 1 results:
Filters: Author is Hashmi, Syed Shahrukh [Clear All Filters]
Whole-exome sequencing reveals an inherited R566X mutation of the epithelial sodium channel β-subunit in a case of early-onset phenotype of Liddle syndrome. Cold Spring Harb Mol Case Stud. 2016 ;2(6):a001255.
.