Genetic screening for pheochromocytoma: should SDHC gene analysis be included?

PGL3 syndrome is caused by mutations in the SDHC gene. At present, only a few families affected by SDHC mutations have been reported in the literature and in each of them the clinical presentation was characterised by paragangliomas located only in the head and neck regions. No evidence of thoracic...

وصف كامل

محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Mannelli, M, Ercolino, T, Giachè, V, Simi, L, Cirami, C, Parenti, G
التنسيق: Artigo
اللغة:Inglês
منشور في: BMJ Group 2007
الموضوعات:
Short Report
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC2597951/
https://ncbi.nlm.nih.gov/pubmed/17557926
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.051045
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