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The British Journal of Dermatology|January 18, 2017
Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier functionA D Zimmer, G-J Kim, A Hotz, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|June 22, 2021
Childhood epidermal necrolysis and erythema multiforme major: a multicentre French cohort study of 62 patientsL Giraud-Kerleroux, N Bellon, A Welfringer-Morin, et al.Pageof 2