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27. A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C disease. Kabzińska D; Niemann A; Drac H; Huber N; Potulska-Chromik A; Hausmanowa-Petrusewicz I; Suter U; Kochański A Neurogenetics; 2011 May; 12(2):145-53. PubMed ID: 21365284 [TBL] [Abstract][Full Text] [Related]
28. A Drosophila model of GDAP1 function reveals the involvement of insulin signalling in the mitochondria-dependent neuromuscular degeneration. López Del Amo V; Palomino-Schätzlein M; Seco-Cervera M; García-Giménez JL; Pallardó FV; Pineda-Lucena A; Galindo MI Biochim Biophys Acta Mol Basis Dis; 2017 Mar; 1863(3):801-809. PubMed ID: 28065847 [TBL] [Abstract][Full Text] [Related]
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