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Erratum: A frame shift mutation in the PMP22 gene in hereditary neuropathy with liability to pressure palsies


Book ID
109915955
Publisher
Nature Publishing Group
Year
1994
Tongue
English
Weight
75 KB
Volume
7
Category
Article
ISSN
1061-4036

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## Abstract Hereditary neuropathy with liability to pressure palsies (HNPP) is associated with a deletion in chromosome 17p 11.2, which includes the gene for the peripheral myelin protein 22 (PMP‐22). A β€œgene dosage” effect is probably the mechanism underlying HNPP, but the amount of PMP‐22 mRNA in