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.
| Original language | English |
|---|---|
| Pages (from-to) | 900-902 |
| Number of pages | 3 |
| Journal | Neurology |
| Volume | 57 |
| Publication status | Published - 1 Jan 2001 |
Fingerprint
Dive into the research topics of 'Limb girdle and facial weakness in female carriers of X-linked myotubular myopathy mutations'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver