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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Familial isolated pheochromocytoma presenting a new mutation in the von Hippel-Lindau gene

Gabriela Sansó1, Maria C Garcia Rudaz, Gloria Levin

  • 1Centro de Investigaciones Endocrinológicas, Hospital de Niños R. Gutiérrez, Buenos Aires, Argentina.

American Journal of Hypertension
|December 21, 2004
PubMed

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