A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2.

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Bibliographic Details
Title: A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2.
Authors: Rossor AM; MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, London, UK., Davidson GL, Blake J, Polke JM, Murphy SM, Houlden H, Innes A, Kalmar B, Greensmith L, Reilly MM
Source: Journal of the peripheral nervous system : JPNS [J Peripher Nerv Syst] 2012 Jun; Vol. 17 (2), pp. 201-5.
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 9704532 Publication Model: Print Cited Medium: Internet ISSN: 1529-8027 (Electronic) Linking ISSN: 10859489 NLM ISO Abbreviation: J Peripher Nerv Syst Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1529-8027
DOI:10.1111/j.1529-8027.2012.00400.x