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.
Artículo
en Chino
| WPRIM
| ID: wpr-399139
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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Idioma:
Chino
Revista:
Chinese Journal of Endocrinology and Metabolism
Año:
2008
Tipo del documento:
Artículo
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