G.P.3.09 Cerebellar ataxia, myopathy and sensorimotor neuropathy associated with a mitochondrial m.8363G>A tRNA(Lys) gene mutation: A clinical and biochemical study

Autor:	Esther Brusse, H. J. M. Smeets, Alex Korsten, I.F.M. de Coo, J.A. Maat-Kievit, G.C. Schoonderwoerd, Debby M.E.I. Hellebrekers
Rok vydání:	2009
Předmět:	Genetics Neurology Cerebellar ataxia Pediatrics Perinatology and Child Health Transfer RNA medicine Sensorimotor neuropathy Neurology (clinical) medicine.symptom Biology Gene mutation Myopathy Genetics (clinical)
Zdroj:	Neuromuscular Disorders. 19:564
ISSN:	0960-8966
DOI:	10.1016/j.nmd.2009.06.067
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f83fe39c5b875ef8d605822baff72ad2 https://doi.org/10.1016/j.nmd.2009.06.067 Zobrazit plný text záznamu Full Text from ScienceDirect