1995•Journal of the Neurological SciencesRequires access

Deletion in chromosome 17p11.2 including the peripheral myelin protein-22 (PMP-22) gene in hereditary neuropathy with liability to pressure palsies

Fujio Umehara, Takashirou Kiwaki, Hiroo Yoshikawa, Tomoya Nishimura, Masanori Nakagawa, Wataru Matsumoto, K. Hashimoto, Shuji Izumo, Yumiko Arimura, Kimiyoshi Arimura, Masaru Kuriyama, M Osame

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Key concepts: Peripheral myelin protein 22, Gene duplication, Myelin, Nerve biopsy, Sural nerve, Gene, Medicine, Peripheral neuropathy