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

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dc.contributor.authorKiykim, Ayca
dc.contributor.authorGarncarz, Wojciech
dc.contributor.authorKarakoc-Aydiner, Elif
dc.contributor.authorOzen, Ahmet
dc.contributor.authorKiykim, Ertugrul
dc.contributor.authorYEŞİL, GÖZDE
dc.contributor.authorBoztug, Kaan
dc.contributor.authorBARIŞ, SAFA
dc.contributor.institutionauthorYEŞİL, GÖZDE
dc.date.accessioned2019-10-05T14:59:31Z
dc.date.available2019-10-05T14:59:31Z
dc.date.issued2016-04-01
dc.identifier10.1111/j.1442-200x.2010.03202.x
dc.identifier.citationKiykim 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.identifier.pubmed26916670
dc.identifier.urihttps://hdl.handle.net/20.500.12645/5171
dc.language.isoen
dc.titleNovel CLPB mutation in a patient with 3-methylglutaconic aciduria causing severe neurological involvement and congenital neutropenia
dc.typeArticle
dspace.entity.typePublication
local.article.journalnamePediatrics international : official journal of the Japan Pediatric Society
local.avesis.id7f35c7be-2f09-4714-8592-47d56ad4d759
local.avesis.response5041
local.indexed.atPubMed
relation.isAuthorOfPublicationb653abbc-327a-4b3b-a227-f3344d8d6b70
relation.isAuthorOfPublication.latestForDiscoveryb653abbc-327a-4b3b-a227-f3344d8d6b70

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