Mutations in exon 7 of the GTP-binding protein G(s)α were not a common cause of pseudohypoparathyroidism with Albright's hereditary osteodystrophy in Japanese

Endocrine Journal

Volumn 44, Issue 4, 1997, Pages 621-625

  Takeda, Kyoko ^a   Yokoyama, Minao ^a   Hashimoto, Kozo ^a   Hiromatsu, Yuji ^b   Yamanaka, Hidekata ^c   Shimizu, Taeko ^d   Sasaki, Masahide ^a  

^a KOCHI MEDICAL SCHOOL   (Japan)

^b Kurume University   (Japan)

^c MIYAZAKI PREFECTURAL MIYAZAKI HOSPITAL   (Japan)

^d TORANOMON HOSPITAL   (Japan)

Author keywords

Albright's hereditary osteodystrophy; G(s) mutation; Hormone resistance; Pseudohypoparathyroidism

Indexed keywords

GUANINE NUCLEOTIDE BINDING PROTEIN;

ADULT; ALBRIGHT SYNDROME; ANALYTIC METHOD; ARTICLE; CASE REPORT; EFFECTOR CELL; EXON; FEMALE; GENE ACTIVATION; GENE MUTATION; HORMONE RESISTANCE; HUMAN; MALE; PROTEIN DENATURATION; PSEUDOHYPOPARATHYROIDISM; SIGNAL TRANSDUCTION;

EID: 0030955308     PISSN: 09188959     EISSN: None     Source Type: Journal    
DOI: 10.1507/endocrj.44.621     Document Type: Article

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