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Updated: Aug 9, 2026

03:45
Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
A novel indel COL7A1 mutation 8068del17insGA causes dominant dystrophic epidermolysis bullosa
D Sawamura1, H Nizeki, S Miyagawa
1Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan. smartdai@med.hokudai.ac.jp
The British Journal of Dermatology
|April 26, 2006
Abstract
No abstract available in PubMed .
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