## Abstract Alterations in peripheral myelin protein 22 (PMP22) expression are associated with a heterogeneous group of hereditary demyelinating peripheral neuropathies. Two mutations at glycine 94, a single guanine insertion or deletion in __PMP22__, result in different reading frameshifts and, co
β¦ LIBER β¦
Aggresome Formation in Neuropathy Models Based on Peripheral Myelin Protein 22 Mutations
β Scribed by Mary C. Ryan; Eric M. Shooter; Lucia Notterpek
- Book ID
- 115641718
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 300 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0969-9961
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