Mutations in SURF1 are important genetic cause of Leigh syndrome in Slovak patients

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Title	Mutations in SURF1 are important genetic cause of Leigh syndrome in Slovak patients
Author	Škopková Martina SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV ^SCOPUS ^RID ^ORCID
Co-authors	Daniš Daniel 1989 SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV
	Brennerová Katarína
	Staník Juraj SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV
	Kolníková Miriam
	Gašperíková Daniela SAVBIOMED ; SAVEXEND - Biomedicínske centrum SAV ^SCOPUS ^RID ^ORCID

Source document	EMBO workshop on Molecular biology of mitochondrial gene expression. P. 60-61. -, 2018 ; EMBO workshop on Molecular biology of mitochondrial gene expression
Language	eng - English
Country	SE - Sweden
Document kind	rozpis článkov z periodík (rzb)
Category	GII - Other publications and documents which is not possible to categorize into classes/categories mentioned above
Year	2018

article

rok vydania	rok metriky	IF	IF Q (best)	SJR	SJR Q (best)
2018

Number of the records: 1