Author/Creator: Scharfe, C - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Scharfe, C

1. A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. Issue 10 (20th October 2003)

Authors:: Horváth, R; Lochmüller, H; Scharfe, C; Do, B H; Oefner, P J; Müller-Höcker, J; Schoser, B G; Pongratz, D; Auer, D P; Jaksch, M
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 10(2003)
Page Start:: 752
Record Type:: Journal Article
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2. Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Issue 11 (1st November 2002)

Authors:: Horváth, R; Scharfe, C; Hoeltzenbein, M; Do, B H; Schröder, C; Warzok, R; Vogelgesang, S; Lochmüller, H; Müller-Höcker, J; Gerbitz, K D; Oefner, P J; Jaksch, M
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 11(2002)
Page Start:: 812
Record Type:: Journal Article
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