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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Bibliographic Details
Main Authors: Codruta Diana Petchesi (Author), Gabriela Ciavoi (Author), Claudia Jurca (Author), Romana Vulturar (Author), Marius Bembea (Author)
Format: Book
Published: Amaltea Medical Publishing House, 2021-09-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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