Human genome variation Journal

Overview

publication venue for

A founder deletion in the TRPM1 gene associated with congenital stationary night blindness and myopia is highly prevalent in Ashkenazi Jews.. 6. 2019
The Qatar genome: a population-specific tool for precision medicine in the Middle East.. 3. 2016

Identity

ISO Abbreviation

Hum Genome Var

Linking ISSN

2054-345X

International Standard Serial Number (ISSN)

2054-345X