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Year | Number of Results |
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2005 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 79669
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A novel homozygous frameshift variant in the C3orf52 gene underlying isolated hair loss in a consanguineous family.
Eur J Dermatol. 2021 Jun 1;31(3):409-411. doi: 10.1684/ejd.2021.4053.
Eur J Dermatol. 2021.
PMID: 34309526
No abstract available.
Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis.
Malki L, Sarig O, Cesarato N, Mohamad J, Canter T, Assaf S, Pavlovsky M, Vodo D, Anis Y, Bihari O, Malovitski K, Gat A, Thiele H, White BEP, Samuelov L, Nanda A, Paller AS, Betz RC, Sprecher E.
Malki L, et al.
Genet Med. 2020 Jul;22(7):1227-1234. doi: 10.1038/s41436-020-0794-5. Epub 2020 Apr 27.
Genet Med. 2020.
PMID: 32336749
Free PMC article.
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Identification and in silico characterization of a novel gene: TPA induced trans-membrane protein.
Chan CY, Salabat MR, Ding XZ, Kelly DL, Talamonti MS, Bell RH Jr, Adrian TE.
Chan CY, et al.
Biochem Biophys Res Commun. 2005 Apr 8;329(2):755-64. doi: 10.1016/j.bbrc.2005.02.037.
Biochem Biophys Res Commun. 2005.
PMID: 15737651
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