A 4-base pair deletion mutation of Gsa gene in a Japanese patient with pseudohypoparathyroidism

Journal of Endocrinological Investigation

Volumn 19, Issue 4, 1996, Pages 236-241

  Yokoyama, M ^a   Takeda, K ^a   Iyota, K ^a   Okabayashi, T ^a   Hashimoto, K ^a  

^a KOCHI MEDICAL SCHOOL   (Japan)

Author keywords

Albright's hereditary osteodystrophy; Gs mutation; Hormone resistance; Pseudohypoparathyroidism; pseudopseudohypoparathyroidism

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN; PEPTIDE FRAGMENT;

ADULT; ALLELE; ARTICLE; CASE REPORT; CHEMISTRY; CODON; DNA BASE COMPOSITION; EXON; GENE DELETION; GENETIC SCREENING; GENETICS; HUMAN; JAPAN; MALE; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; PSEUDOHYPOPARATHYROIDISM;

ADULT; ALLELES; BASE COMPOSITION; BASE SEQUENCE; CODON; EXONS; GENE DELETION; GENETIC SCREENING; GTP-BINDING PROTEINS; HUMANS; JAPAN; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PEPTIDE FRAGMENTS; PSEUDOHYPOPARATHYROIDISM;

EID: 0030114453     PISSN: 03914097     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF03349874     Document Type: Article

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