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Year | Number of Results |
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2018 | 1 |
2019 | 2 |
2020 | 1 |
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PubMed (cited) for id: 619208
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Olmsted syndrome with alopecia universalis caused by heterozygous mutation in PERP.
Br J Dermatol. 2020 Jan;182(1):242-244. doi: 10.1111/bjd.18311. Epub 2019 Sep 8.
Br J Dermatol. 2020.
PMID: 31361044
No abstract available.
Mutations in PERP Cause Dominant and Recessive Keratoderma.
Duchatelet S, Boyden LM, Ishida-Yamamoto A, Zhou J, Guibbal L, Hu R, Lim YH, Bole-Feysot C, Nitschké P, Santos-Simarro F, de Lucas R, Milstone LM, Gildenstern V, Helfrich YR, Attardi LD, Lifton RP, Choate KA, Hovnanian A.
Duchatelet S, et al.
J Invest Dermatol. 2019 Feb;139(2):380-390. doi: 10.1016/j.jid.2018.08.026. Epub 2018 Oct 12.
J Invest Dermatol. 2019.
PMID: 30321533
Free PMC article.
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