A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13

Authors :: Barøy, T.
Pedurupillay, C.R.
Bliksrud, Y.T.
Rasmussen, M.
Holmgren, A.
Vigeland, M.D.
Hughes, T.
Brink, M
Rodenburg, R.J.T.
Nedregaard, B.
Strømme, P.
Frengen, E.
Misceo, D.
Barøy, T.
Pedurupillay, C.R.
Bliksrud, Y.T.
Rasmussen, M.
Holmgren, A.
Vigeland, M.D.
Hughes, T.
Brink, M
Rodenburg, R.J.T.
Nedregaard, B.
Strømme, P.
Frengen, E.
Misceo, D.
Source :: European Journal of Medical Genetics; 342; 346; 1769-7212; 6-7; 59; ~European Journal of Medical Genetics~342~346~~~1769-7212~6-7~59~~
Publication Year :: 2016
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: European Journal of Medical Genetics; 342; 346; 1769-7212; 6-7; 59; ~European Journal of Medical Genetics~342~346~~~1769-7212~6-7~59~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1367167230
Document Type :: Electronic Resource

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