Authors:
HOFMANN S
BEZOLD R
JAKSCH M
OBERMAIERKUSSER B
MERTENS S
KAUFHOLD P
RABL W
HECKER W
GERBITZ KD
Citation: S. Hofmann et al., WOLFRAM (DIDMOAD) SYNDROME AND LEBER HEREDITARY OPTIC NEUROPATHY (LHON) ARE ASSOCIATED WITH DISTINCT MITOCHONDRIAL-DNA HAPLOTYPES, Genomics, 39(1), 1997, pp. 8-18
Authors:
HOFMANN S
BEZOLD R
JAKSCH M
KAUFHOLD P
OBERMAIERKUSSER B
GERBITZ KD
Citation: S. Hofmann et al., ANALYSIS OF THE MITOCHONDRIAL-DNA FROM PATIENTS WITH WOLFRAM (DIDMOAD) SYNDROME, Molecular and cellular biochemistry, 174(1-2), 1997, pp. 209-213
Authors:
HOFMANN S
BEZOLD R
JAKSCH M
KAUFHOLD P
OBERMAIERKUSSER B
GERBITZ KD
Citation: S. Hofmann et al., DISEASE RELEVANCE OF THE SO-CALLED SECONDARY LEBER HEREDITARY OPTIC NEUROPATHY MUTATIONS, American journal of human genetics, 60(6), 1997, pp. 1539-1542
Authors:
JAKSCH M
HOFMANN S
KAUFHOLD P
OBERMAIERKUSSER B
ZIERZ S
GERBITZ KD
Citation: M. Jaksch et al., A NOVEL COMBINATION OF MITOCHONDRIAL TRANSFER-RNA AND ND1 GENE-MUTATIONS IN A SYNDROME WITH MELAS, CARDIOMYOPATHY, AND DIABETES-MELLITUS, Human mutation, 7(4), 1996, pp. 358-360
Authors:
GEMPEL K
BRDICZKA D
KADDURAHDAOUK R
WALLIMANN T
KAUFHOLD P
GERBITZ KD
Citation: K. Gempel et al., THE CREATINE ANALOG CYCLOCREATINE INCREASES INSULIN-SECRETION IN INS-1 CELLS VIA A K-INDEPENDENT MECHANISM( CHANNEL), Diabetologia, 39, 1996, pp. 109-109