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

Xenbase Articles:
(

Denotes literature images)

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

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