Germline mutations in the multiple endocrine neoplasia type 1 gene: Evidence for frequent splicing defects

Human Mutation

Volumn 13, Issue 3, 1999, Pages 175-185

  Mutch, Matthew G ^a   Dilley, William G ^a   Sanjurjo, Francisco ^a   DeBenedetti, Mary K ^a   Doherty, Gerard M ^a   Wells Jr , Samuel A ^a   Goodfellow, Paul J ^a   Lairmore, Terry C ^a,b  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b VETERANS AFFAIRS MEDICAL CENTER   (United States)

Author keywords

MEN1 gene; Menin; Multiple endocrine neoplasia type 1; Splice defects

Indexed keywords

ARTICLE; CANCER GENETICS; CLINICAL ARTICLE; DUODENUM CANCER; FAMILIAL CANCER; FRAMESHIFT MUTATION; HUMAN; HYPOPHYSIS ADENOMA; MISSENSE MUTATION; MULTIPLE ENDOCRINE NEOPLASIA; NEUROENDOCRINE TUMOR; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PANCREAS CANCER; PARATHYROID HYPERPLASIA; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RNA SPLICING;

CHROMOSOMES, HUMAN, PAIR 11; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; DNA PRIMERS; FRAMESHIFT MUTATION; GENETIC SCREENING; GERM-LINE MUTATION; HAPLOTYPES; HUMANS; MODELS, GENETIC; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; MUTATION, MISSENSE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; RNA SPLICING;

EID: 0001960246     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1999)13:3<175::AID-HUMU1>3.0.CO;2-R     Document Type: Article

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