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Genotype-phenotype correlation in multiple endocrine neoplasia type 2

Multiple endocrine neoplasia type 2 is an autosomal-dominant hereditary cancer syndrome caused by missense gain-of-function mutations of the rearranged during transfection proto-oncogene, which encodes the receptor tyrosine kinase, on chromosome 10. It has a strong penetrance of medullary thyroid ca...

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Autors principals: Raue, Friedhelm, Frank-Raue, Karin
Format: Artigo
Idioma:Inglês
Publicat: Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo 2012
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3328821/
https://ncbi.nlm.nih.gov/pubmed/22584709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.6061/clinics/2012(Sup01)13
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