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This page is a summary of: Utility of whole-exome sequencing in detecting novel compound heterozygous mutations in COL7A1
among families with severe recessive dystrophic epidermolysis bullosa in India - implications on diagnosis, prognosis and prenatal testing, Journal of the European Academy of Dermatology and Venereology, August 2018, Wiley,
DOI: 10.1111/jdv.14909.
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