Molekulárně genetická vyšetření u autozomálně dominantních demyelinizačních forem dědičných neuropatií Charcot-Marie-Tooth a u choroby Pelizaeus-Merzbacher
We evaluated the relative frequency of each mode of inheritance in the large group of CMT fam i1ies gathered in the DNA laboratory of the Dept. of Child Neurology of the 2nd Medica! School (including famiJies wi th already detected causal mutations). The frequency of dominant and sporadic forms is a...
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| Format: | Doctoral Thesis |
| Language: | Czech |
| Published: |
2007
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| Online Access: | http://www.nusl.cz/ntk/nusl-287467 |