Epidermolysis bullosa with congenital absence of skin: Clinical and genetic characterization of a 23-case series.

Epidermolysis bullosa with congenital absence of skin: Clinical and genetic characterization of a 23-case series. Clin Genet. 2020 May 07;: Authors: Mariath LM, Santin JT, Frantz JA, Doriqui MJR, Schuler-Faccini L, Kiszewski AE PMID: 32383240 [PubMed - as supplied by publisher]

https://www.ncbi.nlm.nih.gov/pubmed/32383240?dopt=Abstract

Source: Clinical Genetics - May 6, 2020 Category: Genetics & Stem Cells Authors: Mariath LM, Santin JT, Frantz JA, Doriqui MJR, Schuler-Faccini L, Kiszewski AE Tags: Clin Genet Source Type: research

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