| Literature DB >> 15668982 |
Meriel E McEntagart1, Sarah L Reid, Alexandre Irrthum, Alexandre Irtthum, Jenny B Douglas, Keith E D Eyre, Michael J Donaghy, Neil E Anderson, Nazneen Rahman.
Abstract
Hereditary motor and sensory neuropathy type IIC (HMSN IIC) is an autosomal dominant axonal neuropathy. The cardinal features include distal muscle wasting and weakness, vocal cord paralysis, and mild sensory impairment. Recently, HMSN IIC locus was mapped to chromosome 12q23-24. Two families affected by HMSN IIC were identified and evaluated for linkage to this region. Segregation analysis in both families was consistent with linkage to chromosome 12q23-24. Combined analysis generated a multipoint LOD score of 2.1 at marker D12S1583 and refined the HMSN IIC gene interval to The clinical and molecular findings are discussed.Entities:
Mesh:
Year: 2005 PMID: 15668982 DOI: 10.1002/ana.20375
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422