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Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown-Vialetto-Van Laere syndrome

Nalini, A; Pandraud, A; Mok, K; Houlden, H; (2013) Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown-Vialetto-Van Laere syndrome. JOURNAL OF THE NEUROLOGICAL SCIENCES , 334 (1-2) pp. 119-122. 10.1016/j.jns.2013.08.003.

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Type: Article
Title: Madras motor neuron disease (MMND) is distinct from the riboflavin transporter genetic defects that cause Brown-Vialetto-Van Laere syndrome
DOI: 10.1016/j.jns.2013.08.003
Keywords: Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences, Neurosciences & Neurology, Madras motor neuron disease, MMND, Riboflavin receptors, C9ORF72, Brown-Vialetto-Van Laere syndrome, BVVL, PROGRESSIVE BULBAR PARALYSIS, HEXANUCLEOTIDE REPEAT, PONTOBULBAR PALSY, VANLAERE SYNDROME, MUSCULAR-ATROPHY, DEAFNESS, PATTERN, INDIA, INHERITANCE, CHILDHOOD
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Neurodegenerative Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1413051
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