نتائج البحث

Identification of a VHL gene mutation in a Chinese family with Von Hippel‑Lindau syndrome.

• Authors : He Z; Department of Neurosurgery, Hunan Cancer Hospital and The Affiliated Cancer Hospital of Xiangya, School of Medicine, Central South University, Changsha, Hunan 410008, P.R. China.; Xia L

Subjects: Mutation, Missense*; Von Hippel-Lindau Tumor Suppressor Protein/Von Hippel-Lindau Tumor Suppressor Protein/Von Hippel-Lindau Tumor Suppressor Protein/*genetics ; von Hippel-Lindau Disease/von Hippel-Lindau Disease/von Hippel-Lindau Disease/*genetics

• Source: Molecular medicine reports [Mol Med Rep] 2018 Jul; Vol. 18 (1), pp. 435-440. Date of Electronic Publication: 2018 May 04.Publisher: D. A. Spandidos Country of Publication: Greece NLM ID: 101475259 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

تفاصيل العنوان