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A case of epidermolysis bullosa simplex with a newly found missense mutation and polymorphism in the highly conserved helix termination motif among type I keratins, which was previously reported as a pathogenic missense mutation

✍ Scribed by N. Hattori; M. Komine; T. Kaneko; K. Shimazu; Y. Tsunemi; M. Koizumi; J. Goto; T. Hashimoto


Book ID
108668978
Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
110 KB
Volume
155
Category
Article
ISSN
0007-0963

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