Assay of growth hormone receptor gene mutations in children with idiopathic short stature / 中华内分泌代谢杂志
Chinese Journal of Endocrinology and Metabolism
; (12): 254-255, 2008.
Article
em Zh
| WPRIM
| ID: wpr-399139
Biblioteca responsável:
WPRO
ABSTRACT
A homozygous A to G transition (AGT to GGT) in codon 16 of growth hormone receptor (GHR) gene was found in one patient with idiopathic short stature(ISS), resulting in an amino acid change(Ser16Gly). This may be a novel GHR gene mutation; and another novel Arg43Gln GHR gene polymorphism was found in Chinese people.
Texto completo:
1
Base de dados:
WPRIM
Idioma:
Zh
Revista:
Chinese Journal of Endocrinology and Metabolism
Ano de publicação:
2008
Tipo de documento:
Article