PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.

D. Pareyson, S. Botti, A. Sghirlanzoni, F. Taroni

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ASJC Scopus subject areas

@article{a57de7f7ca8942aba07ecd3d6e75ffda,

title = "PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.",

author = "D. Pareyson and S. Botti and A. Sghirlanzoni and F. Taroni",

year = "1997",

month = nov,

language = "English",

volume = "49",

pages = "1478--1479",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams and Wilkins",

number = "5",

}

TY - JOUR

T1 - PMP22 frameshift mutation and hereditary neuropathy with liability to pressure palsies.

AU - Pareyson, D.

AU - Botti, S.

AU - Sghirlanzoni, A.

AU - Taroni, F.

PY - 1997/11

Y1 - 1997/11

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M3 - Article

C2 - 9371959

AN - SCOPUS:0031279393

SN - 0028-3878

VL - 49

SP - 1478

EP - 1479

JO - Neurology

JF - Neurology

IS - 5

ER -