A novel germline mutation of multiple endocrine neoplasia type 1 (MEN 1) gene in a Japanese MEN 1 patient and her daughter

Endocrine Journal

Volumn 46, Issue 2, 1999, Pages 325-329

  Ohye, Hidemi ^a   Sato, Makoto ^a   Matsubara, Shuji ^a   Miyauchi, Akira ^b   Kishi Imai, Keiko ^a   Murao, Koji ^a   Takahara, Jiro ^a  

^a KAGAWA UNIVERSITY   (Japan)

^b KUMA HOSPITAL   (Japan)

Author keywords

Hyperparathyroidism; MEN1 gene; Mutation; Prolactinoma

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; DIAGNOSTIC VALUE; DISEASE COURSE; FEMALE; GASTRINOMA; GENE DELETION; HUMAN; HYPERPARATHYROIDISM; MULTIPLE ENDOCRINE NEOPLASIA; PATHOGENESIS; PEDIGREE; PROLACTINOMA; RADIODIAGNOSIS; RESTRICTION MAPPING;

EID: 0033061737     PISSN: 09188959     EISSN: None     Source Type: Journal    
DOI: 10.1507/endocrj.46.325     Document Type: Article

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