Assignment of microsatellite sequences to the region duplicated in CMT1A (17p12): a useful tool for diagnosis.

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Assignment of microsatellite sequences to the region duplicated in CMT1A (17p12): a useful tool for diagnosis.

Charcot-Marie-Tooth disease type 1A (CMT1A), the most prevalent form of the peripheral hereditary neuropathies, has been associated with a duplication of a genomic segment of 1.5 Mb, located in 17p11.2. Recently, the same segment has been found to be deleted in patients with another peripheral neuropathy, hereditary neuropathy with liability to pressure palsies (HNPP). Highly polymorphic marker...

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ژورنال

عنوان ژورنال: Journal of Medical Genetics

سال: 1995

ISSN: 1468-6244

DOI: 10.1136/jmg.32.3.231