An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPP
E Bellone1, P Balestra, G Ribizzi
1Department of Neurosciences, Ophthalmology and Genetics, Section of Medical Genetics, University of Genova, c/o DIMI-Viale Benedetto XV, 6, 16132 Genova, Italy. ebellone@unige.it
Abstract:
Hereditary neuropathy with liability to pressure palsies (HNPP) is an autosomal dominant, demyelinating neuropathy. Point mutations in the PMP22 gene are a rare cause of HNPP. A novel PMP22 splice site mutation (c.179+1 G-->C) is reported in an HNPP family. By reverse transcriptase-polymerase chain reaction experiments, this mutation was shown to cause the synthesis of an abnormal mRNA in which a premature stop codon probably produces a truncated non-functional protein.
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