Related Experiment Video

Updated: May 23, 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

Lateral medullary syndrome in a boy with hereditary dysfibrinogenemia

Tetsuya Kibe1, Manae Ikeya, Kenji Yokochi

  • 1Department of Pediatrics and Pediatric Neurology, Seirei-Mikatahara General Hospital, Hamamatsu, Shizuoka, Japan. t-kibe@sis.seirei.or.jp

Brain & Development
|March 28, 2012
PubMed

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