Back to Journals » The Application of Clinical Genetics » Volume 13

A Homozygous Truncating Mutation in NALCN Causing IHPRF1: Detailed Clinical Manifestations and a Review of Literature

Total article views   HTML views PDF downloads Totals
8,053 Dovepress* 7,367+ 1,180 8,547
PubMed Central* 686 202 888
Totals 8,053 1,382 9,435
*Since 27 August 2020
Total mentioned Facebook Delicious Reddit Twitter Others
58 0 0 0 2 56

View citations on PubMed Central and Google Scholar