Related Experiment Video

Updated: Aug 6, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

Published on: August 8, 2022

Hunter syndrome: case report and review of literature

Adebola Ogunbiyi1, A O Adeyinka, S O Ogah

  • 1Department of Medicine, University College Hospital, Ibadan.

West African Journal of Medicine
|August 22, 2006
PubMed

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