A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia

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In this Subject: <a title="Anatomy & Physiology" href="/content/subcat?j_subject=157&j_availability=">Anatomy & Physiology ,&nbsp; <a title="Neurology & Psychiatry" href="/content/subcat?j_subject=206&j_availability=">Neurology & Psychiatry
By this author: P.A. Wilkinson ;&nbsp; A.H. Crosby ;&nbsp; C. Turner ;&nbsp; L.J. Bradley ;&nbsp; L. Ginsberg ;&nbsp; N.W. Wood ;&nbsp; A.H. Schapira ;&nbsp; T.T. Warner

Authors: P.A. Wilkinson; A.H. Crosby; C. Turner; L.J. Bradley; L. Ginsberg; N.W. Wood; A.H. Schapira; T.T. Warner

Source: Brain, Volume 127, Number 9, September 2004 , pp. 2148-2148(1)

Publisher: Oxford University Press

Price: $42.29 plus tax (Refund Policy)

Document Type: Research article

DOI: http://dx.doi.org/10.1093/brain/awh299

Publication date: 2004-09-01

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Brain provides researchers and clinicians with the finest original contributions in neurology. Leading studies in neurological science are balanced with practical clinical articles. Its citation rating is one of the highest for neurology journals, and it consistently publishes papers that become classics in the field. The Editorial Board reflects both the journal's truly international readership and wide coverage.