Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia

dc.contributor.author	Kiykim, Ayca
dc.contributor.author	YEŞİL, GÖZDE
dc.contributor.author	Ozen, Ahmet
dc.contributor.author	Karakoc-Aydiner, Elif
dc.contributor.author	Garncarz, Wojciech
dc.contributor.author	BARIŞ, SAFA
dc.contributor.author	Boztug, Kaan
dc.contributor.author	Kiykim, Ertugrul
dc.date.accessioned	2019-10-05T14:59:31Z
dc.date.available	2019-10-05T14:59:31Z
dc.date.issued	2016-04-01
dc.identifier	10.1111/j.1442-200x.2010.03202.x
dc.identifier.uri	https://hdl.handle.net/20.500.12645/5171
dc.language.iso	en
dc.subject	Kiykim A., Garncarz W., Karakoc-Aydiner E., Ozen A., Kiykim E., YEŞİL G., Boztug K., BARIŞ S., -Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia-, Clinical Immunology, cilt.165, ss.1-3, 2016
dc.title	Novel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia
dc.type	Article
local.avesis.response	5041
local.article.journalname	Pediatrics international : official journal of the Japan Pediatric Society

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