A Recurrent Homozygous Nonsense Mutation within the LAMA3 Gene as a Cause of Herlitz Junctional Epidermolysis Bullosa in Patients of Pakistani Ancestry: Evidence for a Founder Effect
- 1 April 1996
- journal article
- case report
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 106 (4) , 781-784
- https://doi.org/10.1111/1523-1747.ep12346349
Abstract
No abstract availableKeywords
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