A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10).
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| Title: | A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10). |
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| Authors: | Reid E; Department of Medical Genetics, Cambridge Institute for Medical Research, University of Cambridge, United Kingdom. ereid@hgmp.mrc.ac.uk, Kloos M, Ashley-Koch A, Hughes L, Bevan S, Svenson IK, Graham FL, Gaskell PC, Dearlove A, Pericak-Vance MA, Rubinsztein DC, Marchuk DA |
| Source: | American journal of human genetics [Am J Hum Genet] 2002 Nov; Vol. 71 (5), pp. 1189-94. Date of Electronic Publication: 2002 Sep 24. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: | Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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