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First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation

BACKGROUND: Neurofibromatosis type 2 (NF2) is a rare autosomal dominant nervous system tumor predisposition disorder caused by constitutive inactivation of one of the two copies of NF2. Meningiomas affect about one half of NF2 patients, and are associated with a higher disease burden. Currently, the...

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محفوظ في:

التفاصيل البيبلوغرافية
الحاوية / القاعدة:	BMC Cancer
المؤلفون الرئيسيون:	Dewan, Ramita, Pemov, Alexander, Dutra, Amalia S., Pak, Evgenia D., Edwards, Nancy A., Ray-Chaudhury, Abhik, Hansen, Nancy F., Chandrasekharappa, Settara C., Mullikin, James C., Asthagiri, Ashok R., Heiss, John D., Stewart, Douglas R., Germanwala, Anand V.
التنسيق:	Artigo
اللغة:	Inglês
منشور في:	BioMed Central 2017
الموضوعات:	Case Report
الوصول للمادة أونلاين:	https://ncbi.nlm.nih.gov/pmc/articles/PMC5307647/ https://ncbi.nlm.nih.gov/pubmed/28193203 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12885-017-3127-6
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First insight into the somatic mutation burden of neurofibromatosis type 2-associated grade I and grade II meningiomas: a case report comprehensive genomic study of two cranial meningiomas with vastly different clinical presentation

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