DEL17P13.1
| DEL17P13.1 | |||||||
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| Aliases | C17DELp13.1Chromosome 17p13.1 deletion syndrome | ||||||
| External IDs | GeneCards: [1] | ||||||
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| Species | Human | Mouse | |||||
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| Location (UCSC) | n/a | n/a | |||||
| PubMed search | [1] | n/a | |||||
| Wikidata | |||||||
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Chromosome 17p13.1 deletion syndrome is a protein in humans that is encoded by the DEL17P13.1 gene.[2][3]
References[]
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Chromosome 17p13.1 deletion syndrome".
- ^ Carvalho CM, Vasanth S, Shinawi M, Russell C, Ramocki MB, Brown CW, et al. (November 2014). "Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes". American Journal of Human Genetics. 95 (5): 565–78. doi:10.1016/j.ajhg.2014.10.006. PMC 4225592. PMID 25439725.
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