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Published in Nature genetics (01.06.2013)
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Protective effects of cardiotrophin-1 adenoviral gene transfer on neuromuscular degeneration in transgenic ALS mice
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Published in Human molecular genetics (01.09.2001)
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Mutations in the β-tubulin gene TUBB2B result in asymmetrical polymicrogyria
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Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium
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A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation
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Published in Neurogenetics (01.05.2010)
Published in Neurogenetics (01.05.2010)
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Mutations in the neuronal β-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects
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Published in Human molecular genetics (15.11.2010)
Published in Human molecular genetics (15.11.2010)
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Mutations in the [beta]-tubulin gene TUBB2B result in asymmetrical polymicrogyria
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Published in Nature genetics (01.06.2009)
Published in Nature genetics (01.06.2009)
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Erratum: Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
Poirier, Karine, Lebrun, Nicolas, Broix, Loic, Tian, Guoling, Saillour, Yoann, Boscheron, Cécile, Parrini, Elena, Valence, Stephanie, Pierre, Benjamin Saint, Oger, Madison, Lacombe, Didier, Geneviève, David, Fontana, Elena, Darra, Franscesca, Cances, Claude, Barth, Magalie, Bonneau, Dominique, Bernadina, Bernardo Dalla, N'Guyen, Sylvie, Gitiaux, Cyril, Parent, Philippe, des Portes, Vincent, Pedespan, Jean Michel, Legrez, Victoire, Castelnau-Ptakine, Laetitia, Nitschke, Patrick, Hieu, Thierry, Masson, Cecile, Zelenika, Diana, Andrieux, Annie, Francis, Fiona, Guerrini, Renzo, Cowan, Nicholas J, Bahi-Buisson, Nadia, Chelly, Jamel
Published in Nature genetics (29.07.2013)
Published in Nature genetics (29.07.2013)
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Journal Article
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly
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Published in Nature genetics (01.08.2013)
Published in Nature genetics (01.08.2013)
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In vivo electrotransfer of the cardiotrophin-1 gene into skeletal muscle slows down progression of motor neuron degeneration in pmn mice
Lesbordes, Jeanne-Claire, Bordet, Thierry, Haase, Georg, Castelnau-Ptakhine, Laetitia, Rouhani, Saïd, Gilgenkrantz, Helène, Kahn, Axel
Published in Human molecular genetics (01.07.2002)
Published in Human molecular genetics (01.07.2002)
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Adenoviral cardiotrophin-1 gene transfer protects pmn mice from progressive motor neuronopathy
Bordet, T, Schmalbruch, H, Pettmann, B, Hagege, A, Castelnau-Ptakhine, L, Kahn, A, Haase, G
Published in The Journal of clinical investigation (01.10.1999)
Published in The Journal of clinical investigation (01.10.1999)
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Neuroanatomical distribution of ARX in brain and its localisation in GABAergic neurons
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Published in Brain research. Molecular brain research. (17.03.2004)
Published in Brain research. Molecular brain research. (17.03.2004)
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Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects
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Published in Human molecular genetics (15.11.2010)
Published in Human molecular genetics (15.11.2010)
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Lysosomal hydrolase activity in chorionic villi and embryonic cells in culture
Poenaru, L, Castelnau, L, Choiset, A, Rouquet, Y, Thepot, F
Published in Human genetics (01.01.1985)
Published in Human genetics (01.01.1985)
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Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy
Besançon, A M, Castelnau, L, Nicolesco, H, Dumez, Y, Poenaru, L
Published in Clinical genetics (01.05.1985)
Published in Clinical genetics (01.05.1985)
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