Severe late onset mitochondrial myopathy caused by TK2 mutations

Autor:	L. Carreño-Gago, E. Vergés Gil, M. Olivé Plana, E. García-Arumí, J. Gascón Bayarri
Rok vydání:	2016
Předmět:	medicine.medical_specialty Endocrinology Neurology Mitochondrial myopathy business.industry Internal medicine Pediatrics Perinatology and Child Health medicine Late onset Neurology (clinical) medicine.disease business Genetics (clinical)
Zdroj:	Neuromuscular Disorders. 26:S178
ISSN:	0960-8966
DOI:	10.1016/j.nmd.2016.06.335
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::2d1a0276d8b77ef4ac3eeaf501fc95a3 https://doi.org/10.1016/j.nmd.2016.06.335 Zobrazit plný text záznamu Full Text from ScienceDirect