ORIGINALES
Características clínicas y moleculares de una familia con síndrome de neoplasia endocrina múltiple tipo 1
Clinical and molecular features in a family with multiple endocrine neoplasia type-1 syndrome
Ángel Cosmea,
, Mariano Álvarezb, Adolfo Beguiristainc, Ana María Cobod, Mercedes Robledoe, María Jesús Aranzadif, Evelia Ojedag, Luis Bujandaa, Unai Goikoetxeaa
Autor para correspondencia
acosme@chdo.osakidetza.net
Dr. A. Cosme. Servicio de Aparato Digestivo. Hospital Donostia. Paseo Dr. Beguiristain, s/n. 20014 San Sebastián. Guipúzcoa. España.
Dr. A. Cosme. Servicio de Aparato Digestivo. Hospital Donostia. Paseo Dr. Beguiristain, s/n. 20014 San Sebastián. Guipúzcoa. España.
a Servicio de Aparato Digestivo. Hospital Donostia. CIBEREHD. Universidad del País Vasco. San Sebastián. Guipúzcoa. España
b Servicio de Endocrinología. Hospital Donostia. San Sebastián. Guipúzcoa. España
c Servicio de Cirugía. Hospital Donostia. San Sebastián. Guipúzcoa. España
d Unidad de Diagnóstico Molecular. Hospital Donostia. San Sebastián. Guipúzcoa. España
e Centro Nacional de Investigaciones Oncológicas. Madrid. CIBERER. España
f Servicio de Anatomía Patológica. Hospital Donostia. San Sebastián. Guipúzcoa. España
g Servicio de Medicina Interna. Hospital Donostia. San Sebastián. Guipúzcoa. España
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