NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD

Literature (1)

Literature for OMIM 614254: NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD

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Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy., Lemke JR,Schütz H,Hentschel J,Depienne C,Nava C,Møller RS,Lal D,Neubauer BA,Nürnberg P,Arnold GL,Bhambhani V,Bartholdi D,Misceo D,Frengen E,Strømme P,Dlugos DJ,Doherty ES,Hoffer MJ,Goldstein A,Rajan DS,Narayanan V,Ramsey K,Schrauwen I,Richholt R,Koeleman BP,Mendonça C,de Kovel CG,De Jonghe P,De Meirleir L,Milh M,Lebrun M,Busa T,Francannet C,Riesch E,Biskup S,Vogt H,Helbig I,Michaud JL,Laube B,Helbig KL,Courage C,Kurlemann G,Pedurupillay CR,Belnap N,Hardies K,Badens C,Piton A,Dorn T,Syrbe S,Heyne HO,Thiele H,Ruivenkamp CA,Geider K,Hjalgrim H,Bijlsma EK,Heron D,Sá J,Weckhuysen S, Neurology. June 7, 2016; 86(23):1526-632X.

Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy., Lemke JR,Schütz H,Hentschel J,Depienne C,Nava C,Møller RS,Lal D,Neubauer BA,Nürnberg P,Arnold GL,Bhambhani V,Bartholdi D,Misceo D,Frengen E,Strømme P,Dlugos DJ,Doherty ES,Hoffer MJ,Goldstein A,Rajan DS,Narayanan V,Ramsey K,Schrauwen I,Richholt R,Koeleman BP,Mendonça C,de Kovel CG,De Jonghe P,De Meirleir L,Milh M,Lebrun M,Busa T,Francannet C,Riesch E,Biskup S,Vogt H,Helbig I,Michaud JL,Laube B,Helbig KL,Courage C,Kurlemann G,Pedurupillay CR,Belnap N,Hardies K,Badens C,Piton A,Dorn T,Syrbe S,Heyne HO,Thiele H,Ruivenkamp CA,Geider K,Hjalgrim H,Bijlsma EK,Heron D,Sá J,Weckhuysen S, Neurology. June 7, 2016; 86(23):1526-632X.