PUBLICATIONS of MMG

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Résultats : 4167  publications trouvées.

Nadine, .  et al. 0

Marc; Zelenika

Laurent";AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability
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Leitão, .  et al. 0

Kuechler

Julia
El Chehadeh - issue: Ghoumid - volume: Caumes - pages: Willems.


Françoise, .  et al. 0

Evelyne; Richard

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Biochem Biophys Res Commun. 2006 Feb 17, .  et al. 0

Saywell V

10.1016/j.bbrc.2005.12.080
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Daniel J, .  et al. 0

Riccardi F

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Cardoso C, .  et al. 0

Guerrini R

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a depressed nasal bridge, .  et al. 0

hypertelorism

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Chatron, .  et al. 0

Lewis-Smith

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, .  et al. 0

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J Neurosci. 2005 Dec 14, .  et al. 0

Viemari JC

10.1523/JNEUROSCI.4373-05.2005
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Villard L. "Mol Neurobiol. 2015 Aug, .  et al. 0

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El-Waly B, .  et al. 0

Moncla A

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, .  et al. 0

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, .  et al. 0

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Laurent", .  et al. 0

KCNQ2 models have been developed to elucidate pathological mechanisms and to identify new therapeutic targets. The diversity of Kcnq2 mouse models has proven invaluable to access neuronal networks and evaluate the associated cognitive deficits. This review summarizes the available models and their contribution to our current understanding of KCNQ2 epileptic disorders.;2022-11;04/08/2025 08:04;0

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which would constitute a previously undescribed mutational mechanism.", .  et al. 0

Inc.;;;;;;Place: United States PMID: 17676597

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Am J Med Genet A. 2005 Nov 1, .  et al. 0

Chabrol B

10.1002/ajmg.a.30882
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Borloz E, .  et al. 0

Seve M

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Balzamo E, .  et al. 0

Legeai-Mallet L

Philip N.;"Hum Mutat. 2007 Dec;28(12):1183-8. doi: 10.1002/humu.20611.";Moncla A;Hum Mutat;2007;07/08/2007;;;10.1002/humu.20611
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Florence, .  et al. 0

Gisèle; Michon

Alexandra; Mignot
Fabienne; Lesca - issue: Damien; Trauffler - volume: Adeline; Badens - pages: Estelle; De La Vaissière.