A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature
Karimi, Amir Hossein, Karimi, Mohammad Reza, Farnia, Poopak, Parvini, Farshid, Foroutan, MajidVolume:
Volume 13
Journal:
The Application of Clinical Genetics
DOI:
10.2147/TACG.S261781
Date:
August, 2020
File:
PDF, 1.47 MB
2020