Screening of mutations in NOL3 in a myoclonic syndromes series

Journal of Neurology

Volumn 261, Issue 9, 2014, Pages 1830-1831

  Macerollo, A ^a   Mencacci, N E ^a   Erro, R ^a   Cordivari, C ^a   Edwards, M J ^a   Wood, N W ^a   Bhatia, Kailash P ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

APOPTOSIS REGULATORY PROTEIN; MUSCLE PROTEIN; NOL3 PROTEIN, HUMAN;

AGED; BRAIN CORTEX; ELECTROENCEPHALOGRAPHY; FEMALE; GENETIC SCREENING; GENETICS; HUMAN; MALE; MIDDLE AGED; MISSENSE MUTATION; MYOCLONUS; PATHOPHYSIOLOGY; PHENOTYPE; SYNDROME;

AGED; APOPTOSIS REGULATORY PROTEINS; CEREBRAL CORTEX; ELECTROENCEPHALOGRAPHY; FEMALE; GENETIC TESTING; HUMANS; MALE; MIDDLE AGED; MUSCLE PROTEINS; MUTATION, MISSENSE; MYOCLONUS; PHENOTYPE; SYNDROME;

EID: 84939895989     PISSN: 03405354     EISSN: 14321459     Source Type: Journal    
DOI: 10.1007/s00415-014-7463-z     Document Type: Letter

References (6)

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