Clinical utility gene card for: Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with/without severe ocular involvement

Saved in:
Bibliographic Details
Published in:European journal of human genetics : EJHG 2015-06, Vol.23 (6), p.889-889
Main Authors: Claverie-Martín, Félix, Vargas-Poussou, Rosa, Müller, Dominik, García-Nieto, Víctor
Format: Article
Language:English
Subjects:
Claudins - genetics
Clinical Utility Gene Card
Eye Diseases, Hereditary - diagnosis
Eye Diseases, Hereditary - genetics
Female
Genes
Humans
Male
Renal Tubular Transport, Inborn Errors - diagnosis
Renal Tubular Transport, Inborn Errors - genetics
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:
ISSN:1018-4813
1476-5438
DOI:10.1038/ejhg.2014.176