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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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COL7A1 mutational analysis in Korean patients with dystrophic epidermolysis bullosa
1Department of Dermatology and Cutaneous Biology Research Institute, Yonsei University College of Medicine, Yongdong Severance Hospital, 146-92 Dogok-dong, Kangnam-gu, Seoul 135-720, Korea.
The British Journal of Dermatology
|October 6, 2007
Abstract
No abstract available in PubMed .

