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Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14

McEntagart, M; Norton, N; Williams, H; Teare, MD; Dunstan, M; Baker, P; Houlden, H; Reilly, M; Wood, N; Harper, PS; et al. McEntagart, M; Norton, N; Williams, H; Teare, MD; Dunstan, M; Baker, P; Houlden, H; Reilly, M; Wood, N; Harper, PS; Futreal, PA; Williams, N; Rahman, N (2001) Localization of the gene for distal hereditary motor neuronopathy VII (dHMN-VII) to chromosome 2q14. AMERICAN JOURNAL OF HUMAN GENETICS, 68 (5). 1270 - 1276 (7). ISSN 0002-9297 https://doi.org/10.1086/320122
SGUL Authors: McEntagart, Meriel

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Item Type: Article
Additional Information: PubMed ID: 11294660
Keywords: Chromosome Mapping, Chromosomes, Human, Pair 2, Female, Founder Effect, Genes, Dominant, Genetic Linkage, Haplotypes, Homeodomain Proteins, Humans, Lod Score, Male, Microsatellite Repeats, Muscular Atrophy, Spinal, Pedigree, Peptides, Vocal Cords, Wales, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, SPINAL MUSCULAR-ATROPHY, VOCAL CORD PARALYSIS, MARIE-TOOTH-DISEASE, SENSORY NEUROPATHY, FORM, CMT2D, 7P
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: AMERICAN JOURNAL OF HUMAN GENETICS
ISSN: 0002-9297
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Dates:
DateEvent
1 May 2001Published
Web of Science ID: WOS:000168171200020
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URI: https://openaccess.sgul.ac.uk/id/eprint/2602
Publisher's version: https://doi.org/10.1086/320122

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