File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Clinical and electrophysiological features in Chinese patients with Kennedy's disease

TitleClinical and electrophysiological features in Chinese patients with Kennedy's disease
Authors
KeywordsElectrophysiology
Genetics
Kennedy's disease
Trinucleotide repeats
Issue Date2004
PublisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/clineuro
Citation
Clinical Neurology And Neurosurgery, 2004, v. 106 n. 4, p. 309-312 How to Cite?
AbstractKennedy's disease is a X-linked neuromuscular disorder caused by an expanded trinucleotide repeat in the androgen receptor gene. To ascertain the clinical diagnosis of Kennedy's disease in a Chinese population, we used a rapid, accurate PCR-based sizing method for the CAG repeat allelotype. The clinical and electrophysiological features of affected patients are described. The CAG repeats ranged from 43 to 53 and were inversely correlated with the age of onset (r=-0.63; P<0.005). © 2004 Elsevier B.V. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/79878
ISSN
2021 Impact Factor: 1.885
2020 SCImago Journal Rankings: 0.587
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorHui, ACFen_HK
dc.contributor.authorCheung, PTen_HK
dc.contributor.authorTang, ASYen_HK
dc.contributor.authorFu, Men_HK
dc.contributor.authorWong, Len_HK
dc.contributor.authorKay, Ren_HK
dc.date.accessioned2010-09-06T07:59:46Z-
dc.date.available2010-09-06T07:59:46Z-
dc.date.issued2004en_HK
dc.identifier.citationClinical Neurology And Neurosurgery, 2004, v. 106 n. 4, p. 309-312en_HK
dc.identifier.issn0303-8467en_HK
dc.identifier.urihttp://hdl.handle.net/10722/79878-
dc.description.abstractKennedy's disease is a X-linked neuromuscular disorder caused by an expanded trinucleotide repeat in the androgen receptor gene. To ascertain the clinical diagnosis of Kennedy's disease in a Chinese population, we used a rapid, accurate PCR-based sizing method for the CAG repeat allelotype. The clinical and electrophysiological features of affected patients are described. The CAG repeats ranged from 43 to 53 and were inversely correlated with the age of onset (r=-0.63; P<0.005). © 2004 Elsevier B.V. All rights reserved.en_HK
dc.languageengen_HK
dc.publisherElsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/clineuroen_HK
dc.relation.ispartofClinical Neurology and Neurosurgeryen_HK
dc.rightsClinical Neurology and Neurosurgery. Copyright © Elsevier BV.en_HK
dc.subjectElectrophysiologyen_HK
dc.subjectGeneticsen_HK
dc.subjectKennedy's diseaseen_HK
dc.subjectTrinucleotide repeatsen_HK
dc.titleClinical and electrophysiological features in Chinese patients with Kennedy's diseaseen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0303-8467&volume=106&spage=309&epage=312&date=2004&atitle=Clinical+and+electrophysiological+features+in+Chinese+patients+with+Kennedy%27s+diseaseen_HK
dc.identifier.emailCheung, PT:ptcheung@hkucc.hku.hken_HK
dc.identifier.authorityCheung, PT=rp00351en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/j.clineuro.2004.02.002en_HK
dc.identifier.pmid15297006-
dc.identifier.scopuseid_2-s2.0-3543107252en_HK
dc.identifier.hkuros127701en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-3543107252&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume106en_HK
dc.identifier.issue4en_HK
dc.identifier.spage309en_HK
dc.identifier.epage312en_HK
dc.identifier.isiWOS:000223522500008-
dc.publisher.placeNetherlandsen_HK
dc.identifier.scopusauthoridHui, ACF=7102453810en_HK
dc.identifier.scopusauthoridCheung, PT=7202595465en_HK
dc.identifier.scopusauthoridTang, ASY=36861623800en_HK
dc.identifier.scopusauthoridFu, M=36955266800en_HK
dc.identifier.scopusauthoridWong, L=8622252600en_HK
dc.identifier.scopusauthoridKay, R=7203026797en_HK
dc.identifier.issnl0303-8467-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats