reference/13637279

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/13637279

Outgoing Links

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publicationName	Genetics in medicine : official journal of the American College of Medical Genetics
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bibliographicCitation	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. Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis. Genetics in Medicine. 2020 Jul;22(7):1227–34. doi: 10.1038/s41436-020-0794-5.
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date	202007
identifier	https://pubmed.ncbi.nlm.nih.gov/32336749 https://pubmed.ncbi.nlm.nih.gov/PMC7405639 https://doi.org/10.1038/s41436-020-0794-5
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis
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