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
Full text not available from this repository.
| Item Type: |
Article
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| 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 |
| Related URLs: |
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| Dates: |
| Date | Event |
|---|
| 1 December 2002 | Published |
|
| Web of Science ID: |
WOS:000179631300032 |
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| URI: |
https://openaccess.sgul.ac.uk/id/eprint/423 |
| Publisher's version: |
https://doi.org/10.1136/jnnp.73.6.762 |
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