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

McEntagart, M; Dunstan, M; Bell, C; Boltshauser, E; Donaghy, M; Harper, P S; Williams, N; Teare, M D; Rahman, N

McEntagart, M; Dunstan, M; Bell, C; Boltshauser, E; Donaghy, M; Harper, P S; Williams, N; Teare, M D; Rahman, N.

Affiliation

McEntagart M; Institute of Medical Genetics, University Hospital of Wales, Cardiff, UK.

J Neurol Neurosurg Psychiatry ; 73(6): 762-5, 2002 Dec.

Article in En | MEDLINE | ID: mdl-12438487

Subject(s)

Charcot-Marie-Tooth Disease/genetics; Genetic Heterogeneity; Muscle Weakness/genetics; Vocal Cord Paralysis/genetics; Charcot-Marie-Tooth Disease/classification; Charcot-Marie-Tooth Disease/diagnosis; Chromosome Mapping; Chromosomes, Human, Pair 2; DNA Mutational Analysis; Deafness/classification; Deafness/diagnosis; Deafness/genetics; Female; Genetic Markers/genetics; Genetic Testing; Humans; Lod Score; Male; Muscle Weakness/classification; Muscle Weakness/diagnosis; Pedigree; Vocal Cord Paralysis/classification; Vocal Cord Paralysis/diagnosis

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Charcot-Marie-Tooth Disease / Vocal Cord Paralysis / Genetic Heterogeneity / Muscle Weakness Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2002 Document type: Article Affiliation country: United kingdom

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google