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Germ-Line Mutation Analysis in Patients with Multiple Endocrine Neoplasia Type 1 and Related Disorders

✍ Scribed by Sophie Giraud; Chang X. Zhang; Olga Serova-Sinilnikova; Virginie Wautot; Janine Salandre; Nathalie Buisson; Christine Waterlot; Catherine Bauters; Nicole Porchet; Jean-Pierre Aubert; Philippe Emy; Guillaume Cadiot; Brigitte Delemer; Olivier Chabre; Patricia Niccoli; Frédéric Leprat; Francoise Duron; Brigitte Emperauger; Patrick Cougard; Pierre Goudet; Emile Sarfati; Jean-Paul Riou; Sylvie Guichard; Michel Rodier; Alain Meyrier; Philippe Caron; Marie-Christine Vantyghem; Michel Assayag; Jean-Louis Peix; Michel Pugeat; Vincent Rohmer; Michel Vallotton; Gilbert Lenoir; Patrick Gaudray; Charles Proye; Bernard Conte-Devolx; Philippe Chanson; Yin Y. Shugart; David Goldgar; Arnaud Murat; Alain Calender


Book ID
117852496
Publisher
American Society of Human Genetics
Year
1998
Tongue
English
Weight
779 KB
Volume
63
Category
Article
ISSN
0002-9297

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Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by tumors in parathyroids, enteropancreatic endocrine tissues, anterior pituitary, and other tissues. The gene for MEN1 has recently been cloned and shown to code for a 610-amino acid protein of enigmatic func