Novel 1113delC menin gene mutation in a Polish family with multiple endocrine neoplasia type 1 syndrome

European Journal of Internal Medicine

Volumn 17, Issue 6, 2006, Pages 447-449

  Chudek, Jerzy ^a   Piecha, Grzegorz ^a   Nieszporek, Teresa ^a   Marini, Francesca ^b   Brandi, Maria Luisa ^b   Wiecek, Andrzej ^a  

^a MEDICAL UNIVERSITY OF SILESIA   (Poland)

^b UNIVERSITY OF FLORENCE   (Italy)

Author keywords

Menin; Multiple endocrine neoplasia type 1; Mutation

Indexed keywords

BROMOCRIPTINE; GLUCOSE; PEPTIDE;

ADULT; ARTICLE; CASE REPORT; CODON; EXON; FAMILY HISTORY; FRAMESHIFT MUTATION; GENE; GENE MUTATION; HUMAN; HYPERCALCEMIA; HYPOGLYCEMIA; INSULINOMA; LITHOTRIPSY; MALE; MEN 1 GENE; MENIN GENE; MISSENSE MUTATION; MULTIPLE ENDOCRINE NEOPLASIA; NEPHROLITHIASIS; PANCREAS RESECTION; PARATHYROIDECTOMY; POLAND; PRIMARY HYPERPARATHYROIDISM; PROLACTINOMA; SIBLING; ULTRASONIC LITHOTRIPSY;

EID: 33750014050     PISSN: 09536205     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ejim.2006.02.017     Document Type: Article

References (6)

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