Distal axonopathy in peripheral nerves of PMP22-mutant mice
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چکیده
منابع مشابه
Distal axonopathy in peripheral nerves of PMP22-mutant mice.
A partial duplication of chromosome 17 is associated with Charcot-Marie-Tooth disease type 1A (CMT1A), a demyelinating peripheral neuropathy that causes progressive distal muscle atrophy and sensory impairment. Trisomic expression of peripheral myelin protein 22 (PMP22) whose gene is contained within the duplicated region is considered to be responsible for the disease. By using recombinant gen...
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ژورنال
عنوان ژورنال: Brain
سال: 1999
ISSN: 1460-2156,0006-8950
DOI: 10.1093/brain/122.8.1563