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J Küsel

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The British Journal of Dermatology|July 7, 2019
Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosisL Frommherz, J Küsel, A Zimmer, et al.
The British Journal of Dermatology|July 20, 2018
Mosaicism due to postzygotic mutations in women with focal dermal hypoplasiaL Heinz, E Bourrat, P Vabres, et al.
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.
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Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
The British Journal of Dermatology|July 7, 2019
Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosisL Frommherz, J Küsel, A Zimmer, et al.
The British Journal of Dermatology|July 20, 2018
Mosaicism due to postzygotic mutations in women with focal dermal hypoplasiaL Heinz, E Bourrat, P Vabres, et al.
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.
Pageof 1