Detección de una mutación no estándar en el proto-oncogen ret por mutagénesis dirigida. / [Detection of a non-standard mutation in the ret protoncogene by site directed mutagenesis]
Medicina [B Aires]
; 65(1): 41-6, 2005.
Article
in Spanish
| BINACIS
| ID: bin-38376
Responsible library:
AR2.1
ABSTRACT
MEN2A is an autosomic dominant disease, characterized by medullary thyroid cancer, pheochromocytoma and parathyroid hyperplasia. Mutations in the ret proto-oncogene are associated with this disease, with almost 100
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Collection:
National databases
/
Argentina
Database:
BINACIS
Type of study:
Diagnostic study
Language:
Spanish
Journal:
Medicina [B Aires]
Year:
2005
Document type:
Article
