Application of the next generation sequencing technolgy in identification of mitochondrial mutations in patients with congenital heart defects

dc.contributor.author	Abacı, Neslihan
dc.contributor.author	Çakiris, Aris
dc.contributor.author	Üstek, Duran
dc.contributor.author	Sırma Ekmekci, Sema
dc.contributor.author	Tansel, Türkan
dc.contributor.author	Arıkan, Muzaffer
dc.contributor.author	Gök, E
dc.date.accessioned	2021-03-03T17:54:07Z
dc.date.available	2021-03-03T17:54:07Z
dc.identifier.citation	Abacı N., Arıkan M., Gök E., Çakiris A., Sırma Ekmekci S., Tansel T., Üstek D., "Application of the next generation sequencing technolgy in identification of mitochondrial mutations in patients with congenital heart defects", European Human Genetic Conference, Milan, İtalya, 31 Mayıs 2014, cilt.22, ss.117
dc.identifier.other	vv_1032021
dc.identifier.other	av_4c1dd9af-5274-4b52-9d1d-5f01467c1e2c
dc.identifier.uri	http://hdl.handle.net/20.500.12627/54561
dc.language.iso	eng
dc.subject	Klinik Tıp (MED)
dc.subject	Sağlık Bilimleri
dc.title	Application of the next generation sequencing technolgy in identification of mitochondrial mutations in patients with congenital heart defects
dc.type	Bildiri
dc.contributor.department	, ,
dc.identifier.volume	22
dc.contributor.firstauthorID	806014

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