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Whole Exome Sequencing Identifies a Homozygous POLG2 Missense Variant in an adult patient presenting with movement disorders and Mitochondrial DNA Depletion

Document Type

Journal

Author

Dosekova, P.; Habalova, V.; Skirkova, M.; Han, V.; Mosejova, A.; Gdovinova, Z.; Skorvanek, M.; Ploski, R.

Source

MOVEMENT DISORDERS; OCT 2019, 34 pS175-pS175, 1p. Supplement: 2

Subject

Language

English

ISSN

15318257

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Find it@PNU

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