Condition: SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES


rs139036657 in NPR2 gene and SHORT STATURE WITH NONSPECIFIC SKELETAL ABNORMALITIES PMID 24471569 2014 Identification and functional characterization of two novel NPR2 mutations in Japanese patients with short stature.

PMID 24001744 2013 Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature in patients initially classified as idiopathic short stature.