Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.
Johnson, Janel O.; Gibbs, J. Raphael; Megarbane, Andre; Urtizberea, J. Andoni; Hernandez, Dena G.; Foley, A. Reghan; Arepalli, Sampath; Pandraud, Amelie; Simón-Sánchez, Javier; Clayton, Peter; Reilly, Mary M.; Muntoni, Francesco; Abramzon, Yevgeniya; Houlden, Henry; Singleton, Andrew B.; Brain: A Journal of Neurology, 2012, vol. 135, issue 9, p 2875, ISSN 00068950. ISBN 14602156.

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