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- W2347440083 abstract "Mutations in human genes may cause peripheral neuropathies,which are collectively called as Charcot-Marie-Tooth disease(CMT) . CMT affects one in 2 500 people,and is one of the most common inherited neurological disorders. There are now over 53 chromosomal loci and 35 specific genes that are linked to different types of CMT. Peripheral myelin protein-22(PMP22) was discovered to be causal gene for the largest group of patients with CMT. The biology of PMP22 and the pathophysiology of its related diseases,were reviewed here." @default.
- W2347440083 created "2016-06-24" @default.
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- W2347440083 date "2010-01-01" @default.
- W2347440083 modified "2023-09-24" @default.
- W2347440083 title "PMP22 and its related diseases" @default.
- W2347440083 hasPublicationYear "2010" @default.
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