Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and children

Authors :: Stewart, J.D.
Tennant, S.
Powell, H.
Pyle, A.
Blakely, E.L.
He, L.
Hudson, G.
Roberts, M.
du Plessis, D.
Gow, D.
Mewasingh, L.D.
Hanna, M.G.
Omer, S.
Morris, A.A.
Roxburgh, R.
Livingston, J.H.
McFarland, R.
Turnbull, D.M.
Chinnery, P.F.
Taylor, R.W.
Source :: Journal of Medical Genetics. March, 2009, Vol. 46 Issue 3, p209, 6 p.
Publication Year :: 2009

Subjects :: Gene mutations -- Research
Mitochondrial diseases -- Genetic aspects
Mitochondrial diseases -- Development and progression
Mitochondrial diseases -- Research
Neurologic manifestations of general diseases -- Genetic aspects
Neurologic manifestations of general diseases -- Research
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