A novel, complex heterozygous mutation within Gsα gene in patient with McCune-Albright syndrome

Endocrine

Volumn 18, Issue 2, 2002, Pages 121-128

  Song, Huai Dong ^a   Chen, Feng Ling ^a   Shi, Wen Jing ^a   Wang, Shu ^a   Zhang, Qun ^a   Hu, Ren Ming ^a   Chen, Jia Lun ^a  

^a SHANGHAI SECOND MEDICAL UNIVERSITY   (China)

Author keywords

Gene mutation; Gs gene; McCune Albright syndrome

Indexed keywords

ARGININE; CYSTEINE; GLYCINE; HISTIDINE; STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN;

ADOLESCENT; ALBRIGHT SYNDROME; AMINO ACID SUBSTITUTION; ARTICLE; BONE DISEASE; CASE REPORT; CHINESE; FIBROUS DYSPLASIA; GENE MUTATION; HETEROZYGOSITY; HUMAN; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; SIGNAL TRANSDUCTION;

EID: 0036658052     PISSN: 1355008X     EISSN: 15590100     Source Type: Journal    
DOI: 10.1385/ENDO:18:2:121     Document Type: Article

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