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Year | Number of Results |
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2000 | 1 |
2014 | 1 |
2018 | 1 |
2024 | 0 |
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Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.
Br J Dermatol. 2014 Dec;171(6):1521-4. doi: 10.1111/bjd.13176. Epub 2014 Oct 26.
Br J Dermatol. 2014.
PMID: 24909267
A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23.
Lee YA, Stevens HP, Delaporte E, Wahn U, Reis A.
Lee YA, et al.
Am J Hum Genet. 2000 Jan;66(1):326-30. doi: 10.1086/302718.
Am J Hum Genet. 2000.
PMID: 10631162
Free PMC article.
No abstract available.
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SMARCAD1 Haploinsufficiency Underlies Huriez Syndrome and Associated Skin Cancer Susceptibility.
Günther C, Lee-Kirsch MA, Eckhard J, Matanovic A, Kerscher T, Rüschendorf F, Klein B, Berndt N, Zimmermann N, Flachmeier C, Thuß T, Lucas N, Marenholz I, Esparza-Gordillo J, Hübner N, Traupe H, Delaporte E, Lee YA.
Günther C, et al.
J Invest Dermatol. 2018 Jun;138(6):1428-1431. doi: 10.1016/j.jid.2018.01.015. Epub 2018 Feb 1.
J Invest Dermatol. 2018.
PMID: 29409814
Free article.
No abstract available.
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