Open AccessReply: Novel peripheral myelin protein 22 (PMP22) micromutations associated with variable phenotypes in Greek patients with Charcot-Marie-Tooth disease
Author(s) -
Gian Maria Fabrizi,
Federica Taioli,
Tiziana Cavallaro
Publication year - 2012
Publication title -
brain
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.142
H-Index - 336
eISSN - 1460-2156
pISSN - 0006-8950
DOI - 10.1093/brain/aws035
Subject(s) - peripheral myelin protein 22 , medicine , disease , phenotype , haploinsufficiency , neurology , genetics , pathology , biology , gene , psychiatry
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