Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1).
Author
Wen, DBalacco, D L
Bardhan, A
Harper, N
Walsh, D
Ryan, G
Liu, L
Guy, A
McGrath, J A
Ogboli, M
Heagerty, A H M
Publication date
2021-11-21
Metadata
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Wen D, Balacco DL, Bardhan A, Harper N, Walsh D, Ryan G, Liu L, Guy A, McGrath JA, Ogboli M, Heagerty AHM. Localized autosomal recessive epidermolysis bullosa simplex arising from a novel homozygous frameshift mutation in DST (BPAG1). Clin Exp Dermatol. 2022 Feb;47(2):497-502. doi: 10.1111/ced.14917. Epub 2021 Nov 21Type
ArticleAdditional Links
https://academic.oup.com/cedPMID
34806203Publisher
Oxford University Pressae974a485f413a2113503eed53cd6c53
10.1111/ced.14917