| 1 | MMVC2, RAD51
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| Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations.
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| Franz EA, Chiaroni-Clarke R, Woodrow S, Glendining KA, Jasoni CL, Robertson SP, Gardner RJ, Markie D.
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| J Neurol Sci 351(1-2):140-5. doi: 10.1016/j.jns.2015.03.006.
2015
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| 2 | MMVC2, RAD51
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| Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases.
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| Méneret A, Depienne C, Riant F, Trouillard O, Bouteiller D, Cincotta M, Bitoun P, Wickert J, Lagroua I, Westenberger A, Borgheresi A, Doummar D, Romano M, Rossi S, Defebvre L, De Meirleir L, Espay AJ, Fiori S, Klebe S, Quélin C, Rudnik-Schöneborn S, Plessis G, Dale RC, Sklower Brooks S, Dziezyc K, Pollak P, Golmard JL, Vidailhet M, Brice A, Roze E.
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| Neurology 82(22):1999-2002. doi: 10.1212/WNL.0000000000000477.
2014
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| 3 | MMVC2, RAD51
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| RAD51 Haploinsufficiency Causes Congenital Mirror Movements in Humans.
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| Depienne C, Bouteiller D, Méneret A, Billot S, Groppa S, Klebe S, Charbonnier-Beaupel F, Corvol JC, Saraiva JP, Brueggemann N, Bhatia K, Cincotta M, Brochard V, Flamand-Roze C, Carpentier W, Meunier S, Marie Y, Gaussen M, Stevanin G, Wehrle R, Vidailhet M, Klein C, Dusart I, Brice A, Roze E.
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| Am J Hum Genet 90(2):301-7. Epub 2012 Feb 2.
2012
|