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The lethal phenotype of a homozygous nonsense mutation in the lamin A/C gene
B G M van Engelen1, A Muchir, C J Hutchison
1Neuromuscular Centre, Nijmegen Institute of Neurology and Department of Pathology, University Medical Centre Nijmegen, 6500 HB Nijmegen, The Netherlands. b.vanengelen@neuro.umcn.nl
Abstract:
The authors report the clinical and histologic phenotypes of a LGMD1B family including a newborn child with a homozygous LMNA nonsense mutation (Y259X). At the heterozygous state the nonsense mutation leads to a classic LGMD1B phenotype; the homozygous LMNA nonsense mutation causes a lethal phenotype.
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