The Human COX10 Gene is Disrupted During Homologous Recombination Between the 24 kb Proximal and Distal CMT1A-REPs

By Reiter Lawrence T.  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-09 ,pp. : 1595-1603

Oxford University Press

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Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPP

By Lopes Judith   Tardieu Sandrine   Silander Kaisa  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2285-2292

Oxford University Press

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Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements

By Ballif Blake   Wakui Keiko   Gajecka Marzena   Shaffer Lisa  

Human Genetics, Vol. 114, Iss. 2, 2004-01 ,pp. : 198-206

Springer Publishing Company

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Primate Origin of the CMT1A-REP Repeat and Analysis of a Putative Transposon-Associated Recombinational Hotspot

By Kiyosawa Hidenori   Chance Phillip F.  

Human Molecular Genetics, Vol. 5, Iss. 6, 1996-01 ,pp. : 745-753

Oxford University Press

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Charcot–Marie–Tooth disease CMT4A: GDAP1 increases cellular glutathione and the mitochondrial membrane potential

By Noack Rebecca   Frede Svenja   Albrecht Philipp   Henke Nadine   Pfeiffer Annika   Knoll Katrin   Dehmel Thomas   Meyer zu Hörste Gerd   Stettner Mark   Kieseier Bernd C.   Summer Holger   Golz Stefan   Kochanski Andrzej   Wiedau-Pazos Martina   Arnold Susanne   Lewerenz Jan   Methner Axel  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 150-162

Oxford University Press

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