Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype

dc.contributor.author	DEMİRKESEN, Cüyan
dc.contributor.author	Gibbs, Richard
dc.contributor.author	Lupski, James
dc.contributor.author	ENGİN, Burhan
dc.contributor.author	ÇELİK, Uğur
dc.contributor.author	Gezdirici, Alper
dc.contributor.author	Bayram, Yavuz
dc.contributor.author	Tomasz, Gambin
dc.contributor.author	Karaca, Ender
dc.contributor.author	Shalini, Jhangiani
dc.contributor.author	Barış, Tuğba
dc.date.accessioned	2021-03-03T16:13:04Z
dc.date.available	2021-03-03T16:13:04Z
dc.identifier.citation	Gezdirici A., Bayram Y., ENGİN B., ÇELİK U., Tomasz G., DEMİRKESEN C., Karaca E., Shalini J., Barış T., Gibbs R., et al., "Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype", European Society of Human Genetics (ESHG) Conference, Glasgow, İskoçya, 6 - 09 Haziran 2015, ss.104
dc.identifier.other	vv_1032021
dc.identifier.other	av_4305b362-a177-410c-8818-71520022609e
dc.identifier.uri	http://hdl.handle.net/20.500.12627/48774
dc.language.iso	eng
dc.subject	Klinik Tıp (MED)
dc.subject	Tıp
dc.subject	Sağlık Bilimleri
dc.title	Olmsted syndrome: a novel homozygous TRPV3 mutation with severe phenotype
dc.type	Bildiri
dc.contributor.department	Diğer Kurumlar , ,
dc.contributor.firstauthorID	429331

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