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Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness

McEntagart, M; Dunstan, M; Bell, C; Boltshauser, E; Donaghy, M; Harper, PS; Williams, N; Teare, MD; Rahman, N (2002) Clinical and genetic heterogeneity in peroneal muscular atrophy associated with vocal cord weakness. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 73 (6). 762 - 765 (4). ISSN 0022-3050 https://doi.org/10.1136/jnnp.73.6.762
SGUL Authors: McEntagart, Meriel

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Item Type: Article
Additional Information: PubMed ID: 12438487
Keywords: Charcot-Marie-Tooth Disease, Chromosome Mapping, Chromosomes, Human, Pair 2, DNA Mutational Analysis, Deafness, Female, Genetic Heterogeneity, Genetic Markers, Genetic Testing, Humans, Lod Score, Male, Muscle Weakness, Pedigree, Vocal Cord Paralysis, Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Psychiatry, Surgery, Neurosciences & Neurology, MARIE-TOOTH-DISEASE, HEREDITARY MOTOR, SENSORY NEUROPATHY, POINT MUTATION, PMP22 GENE, PARALYSIS, LOCALIZATION, PHENOTYPE, DEAFNESS, CMT2D
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
ISSN: 0022-3050
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Dates:
DateEvent
1 December 2002Published
Web of Science ID: WOS:000179631300032
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URI: http://openaccess.sgul.ac.uk/id/eprint/423
Publisher's version: https://doi.org/10.1136/jnnp.73.6.762

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