| Literature DB >> 11552027 |
I J Sutton1, J B Winer, A N Norman, S Liechti-Gallati, F MacDonald.
Abstract
Although X-linked myotubular myopathy (XLMTM) is a recessive disorder, heterozygous female carriers of MTM1 mutations may present with limb girdle and facial weakness. It is proposed that manifesting heterozygote females with XLMTM have a skewed pattern of X-chromosome inactivation. However, skewed X-chromosome inactivation was not detected in either the lymphocyte or muscle DNA of a woman who presented with limb girdle/facial weakness and was found to be heterozygous for the R224X mutation.Entities:
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Year: 2001 PMID: 11552027 DOI: 10.1212/wnl.57.5.900
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910