Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins
- 13 June 2006
- journal article
- research article
- Published by Springer Nature in Archives of Dermatological Research
- Vol. 298 (3), 135-137
- https://doi.org/10.1007/s00403-006-0671-3
Abstract
No abstract availableKeywords
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