Hypertrophic cardiomyopathy in noonan syndrome

Article

Abstract: Noonan syndrome is a rare genetic disorder. It has an autosomal dominant and heterogeneous pattern,

Palabras claves:

Cardiopathy, Mutations, Noonan

Autores:

Al-subhi S.S.H., Ana Belén Pérez Proaño, Barrionuevo C.G.L., Juan Alberto Viteri Rodríguez, Santamaría M.A.G.

Fuentes:

scopus