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Marion Coolen, Nami Altin, Karthyayani Rajamani , Giulia Barcia, Aurore POULIET, Patrick Nitschké, Nathalie Boddaert, Antonio Rausell, Lydie Burglen, Vincent Cantagrel
Source : Am J Hum Genet
2022 May 5
Pmid / DOI: 35390279
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Vincent Cantagrel
Source : Am. J. Hum. Genet.
2020 Feb 28
Pmid / DOI: 32109419
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Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy.
Source : J. Clin. Invest.
2019 Nov 20
Pmid / DOI: 30620337
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Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination.
Vincent Cantagrel
Source : Brain
2019 Oct 23
Pmid / DOI: 31501903
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Vincent Cantagrel
Source : Brain
2019 Jul 17
Pmid / DOI: 29878067
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Valérie Malan
Source : Eur. J. Hum. Genet.
2019 Feb 21
Pmid / DOI: 29483668
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Vincent Cantagrel, Nathalie Lefort
Source : Elife
2019 Jan 21
Pmid / DOI: 30311906
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AMPA-receptor specific biogenesis complexes control synaptic transmission and intellectual ability.
Patrick Nitschké, Karine Siquier
Source : Nat Commun
2018 Dec 11
Pmid / DOI: 28675162
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Yves Ville
Source : JAMA
2018 Sep 4
Pmid / DOI: 30120476
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Vincent Cantagrel
Source : Orphanet J Rare Dis
2017 Nov 7
Pmid / DOI: 27146152
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Nadia Bahi-Buisson, Sophie Thomas, Matias Simons, Vincent Cantagrel, Meriem Garfa-Traoré , Patrick Nitschké, Tania Attié-Bitach
Source : Brain
2017 Oct 6
Pmid / DOI: 28969387
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Lydie Burglen
Source : Am J Hum Genet
Pmid / DOI: 35390279
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Source : Eur J Hum Genet
. 2022 Jun;30(6):712-720. doi: 10.1038/s41431-022-01094-x.Pmid / DOI:
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Lydie Burglen
Source : Genet Med.
Pmid / DOI: 32103185
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Vincent Cantagrel
Source : Nature Communications
Pmid / DOI: 33257696