Fate of Schwann Cells in CMT1A and HNPP: Evidence for Apoptosis
نویسندگان
چکیده
منابع مشابه
A Family Harboring CMT1A Duplication and HNPP Deletion
Charcot-Marie-Tooth disease type 1A (CMT1A) is associated with duplication of chromosome 17p11.2-p12, whereas hereditary neuropathy with liability to pressure palsies (HNPP), which is an autosomal dominant neuropathy showing characteristics of recurrent pressure palsies, is associated with 17p11.2-p12 deletion. An altered gene dosage of PMP22 is believed to the main cause underlying the CMT1A a...
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ژورنال
عنوان ژورنال: Journal of Neuropathology & Experimental Neurology
سال: 1998
ISSN: 0022-3069,1554-6578
DOI: 10.1097/00005072-199806000-00009