Activating and inactivating mutations in the human GNAS1 gene

Human Mutation

Volumn 16, Issue 3, 2000, Pages 183-189

  Aldred, Micheala A ^a,b   Trembath, Richard C ^a,b  

^a LEICESTER ROYAL INFIRMARY   (United Kingdom)

^b UNIVERSITY OF LEICESTER   (United Kingdom)

Author keywords

AHO; Albright hereditary osteodystrophy; GNAS1; Gs alpha; MAS; McCune Albright syndrome; Pseudohypoparathyroidism

Indexed keywords

STIMULATORY GUANINE NUCLEOTIDE BINDING PROTEIN;

ALBRIGHT SYNDROME; AMINO ACID SUBSTITUTION; CHROMOSOME 20; ENDOCRINE TUMOR; GENE; GENE ACTIVATION; GENE DELETION; GENE FUNCTION; GENE INACTIVATION; GENE MUTATION; HETEROZYGOSITY LOSS; HUMAN; PRIORITY JOURNAL; REVIEW;

FIBROUS DYSPLASIA, POLYOSTOTIC; GENE EXPRESSION REGULATION, NEOPLASTIC; GTP-BINDING PROTEIN ALPHA SUBUNITS, GS; HUMANS; MUTATION; ONCOGENE PROTEINS;

EID: 0033855731     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/1098-1004(200009)16:3<183::AID-HUMU1>3.0.CO;2-L     Document Type: Review

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