Neurofibromatóza typu 1 a zárodečné mutace genu NF1 u českých pacientů
Neurofibromatosis type 1 (NF1, MIM 162200) is an autosomal dominant disorder affecting about 1 of 3000 live births, involving many cell types and organs, and associated with an increased risk of malignancy, predominantly of the central and peripheral nervous system 1. Tumour development is caused by...
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| Format: | Doctoral Thesis |
| Language: | Czech |
| Published: |
2012
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| Online Access: | http://www.nusl.cz/ntk/nusl-308918 |