Mutational Analysis and mtDNA Haplogroup Characterization in Three Serbian Cases of Mitochondrial Encephalomyopathies and Literature Review

Mitochondrial encephalomyopathies (MEMP) are heterogeneous multisystem disorders frequently associated with mitochondrial DNA (mtDNA) mutations. Clinical presentation varies considerably in age of onset, course, and severity up to death in early childhood. In this study, we performed molecular genet...

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Xehetasun bibliografikoak

Egile Nagusiak:	Phepy G. A. Dawod, Jasna Jancic, Ana Marjanovic, Marija Brankovic, Milena Jankovic, Janko Samardzic, Ayman Gamil Anwar Dawod, Ivana Novakovic, Fayda I. Abdel Motaleb, Vladimir Radlovic, Vladimir S. Kostic, Dejan Nikolic
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	MDPI AG 2021-10-01
Saila:	Diagnostics
Gaiak:	MELAS leigh syndrome mtDNA sanger sequencing mutations haplogroups
Sarrera elektronikoa:	https://www.mdpi.com/2075-4418/11/11/1969
Etiketak:	Etiketa erantsi Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!