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Deletion of the PMP22 gene and hereditary neuropathy with liability to pressure palsies.
Curr Opin Neurol. 1996 Oct;9(5):348-54. doi: 10.1097/00019052-199610000-00006.
Curr Opin Neurol. 1996.
PMID: 8894410
Review.
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion.
Pareyson D, Scaioli V, Taroni F, Botti S, Lorenzetti D, Solari A, Ciano C, Sghirlanzoni A.
Pareyson D, et al.
Neurology. 1996 Apr;46(4):1133-7. doi: 10.1212/wnl.46.4.1133.
Neurology. 1996.
PMID: 8780105
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A 1.5-Mb deletion in 17p11.2-p12 is frequently observed in Italian families with hereditary neuropathy with liability to pressure palsies.
Lorenzetti D, Pareyson D, Sghirlanzoni A, Roa BB, Abbas NE, Pandolfo M, Di Donato S, Lupski JR.
Lorenzetti D, et al.
Am J Hum Genet. 1995 Jan;56(1):91-8.
Am J Hum Genet. 1995.
PMID: 7825607
Free PMC article.
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