Bioethical aspects in type I neurofibromatosis
Type I neurofibromatosis is one of the most common monogenic disorders, being caused by abnormalities of the neurofibromin gene on chromosome 17. About half of the cases are inherited, respecting the autosomal dominant inheritance criteria, the rest are de novo cases. The clinical manifestations are...
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| Main Authors: | , , , , |
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| Format: | Book |
| Published: |
Amaltea Medical Publishing House,
2021-09-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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