Diagnostic and therapeutic process of neurofibromatosis type 1 and type 2
Neurofibromatosis is one of the most common genetic diseases. It is inherited in an autosomal dominant manner. It is divided into two genetically distinct subtypes, characterised by multiple skin lesions and tumours of the peripheral and central nervous system. Neurofibromatosis type 1, or...
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| Asıl Yazarlar: | , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Kazimierz Wielki University
2024-02-01
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| Seri Bilgileri: | Journal of Education, Health and Sport |
| Konular: | |
| Online Erişim: | https://apcz.umk.pl/JEHS/article/view/48531 |
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