An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutation

Journal article

Peer reviewed

P.J. Lamont, R. Jacob, F. Mastaglia and N. Laing

Journal of Neurology, Neurosurgery & Psychiatry, Vol.75(2), pp.343-343

2004

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Letter to the editor

Title: An expansion in the ZNF9 gene causes PROMM in a previously described family with an incidental CLCN1 mutation
Authors/Creators: P.J. Lamont (Author/Creator)
R. Jacob (Author/Creator)
F. Mastaglia (Author/Creator) - Centre for Neuromuscular and Neurological Disorders
N. Laing (Author/Creator) - UWA Centre for Medical Research
Publication Details: Journal of Neurology, Neurosurgery & Psychiatry, Vol.75(2), pp.343-343
Publisher: BMJ Publishing Group
Identifiers: 991005540350307891
Copyright: 2004 BMJ Publishing Group
Murdoch Affiliation: Murdoch University
Language: English
Resource Type: Journal article

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Collaboration types: Domestic collaboration
Citation topics: 1 Clinical & Life Sciences; 1.79 Molecular & Cell Biology - Physiology; 1.79.1811 Myotonic Dystrophy Mechanisms
Web Of Science research areas: Clinical Neurology; Psychiatry; Surgery
ESI research areas: Clinical Medicine