Open AccessTRPM6 Gene Mutation Responsible for Familial Hypomagnesemia with Secondary Hypocalcemia
Author(s) -
Mahmoud Al Hussein,
Shafiqa Saleh,
Sura El Doory,
Mohammed Ali Al Sabbah,
Maysa Saleh
Publication year - 2019
Publication title -
archives of clinical and medical case reports
Language(s) - English
Resource type - Journals
ISSN - 2575-9655
DOI - 10.26502/acmcr.96550055
Subject(s) - hypomagnesemia , endocrinology , medicine , calcium metabolism , homeostasis , parathyroid hormone , mutation , gene mutation , calcium , gene , calcium sensing receptor , biology , genetics , chemistry , magnesium , organic chemistry