Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel-Lindau disease patients.

scientific article published in March 2014

Higher prevalence of novel mutations in VHL gene in Chinese Von Hippel-Lindau disease patients. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1016/J.UROLOGY.2013.09.069
P698PubMed publication ID24581539

P50authorYu FanQ87834654
P2093author name stringNing Zhang
Xi Wang
Dingfang Bu
Kan Gong
Pengjie Wu
Shuanghe Peng
Teng Li
Xianghui Ning
P2860cites workClustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locusQ28242901
Identification of the von Hippel-Lindau disease tumor suppressor geneQ29618644
Central nervous system lesions in von Hippel-Lindau syndromeQ33591720
Von Hippel-Lindau disease: a genetic studyQ33597245
A genetic register for von Hippel-Lindau diseaseQ33683199
LINDAU'S DISEASE. REVIEW OF THE LITERATURE AND STUDY OF A LARGE KINDRED.Q34540867
High frequency of novel germline mutations in the VHL gene in the heterogeneous population of BrazilQ41876493
Germline mutations in the von Hippel-Lindau disease (VHL) gene in mainland Chinese familiesQ43466454
Clinical and mutation analysis of four Chinese families with von Hippel-Lindau diseaseQ44819707
Family history of von Hippel-Lindau disease was uncommon in Chinese patients: suggesting the higher frequency of de novo mutations in VHL gene in these patientsQ44847037
Molecularly genetic analysis of von Hippel-Lindau associated central nervous system hemangioblastoma.Q45966988
A c.464T>a mutation in VHL gene in a Chinese family with VHL syndromeQ46133879
Familial and genetic researches on three Chinese families with von Hippel-Lindau diseaseQ46169843
Mosaicism in von Hippel-Lindau disease with severe renal manifestations.Q53121842
Bilateral pheochromocytoma as first presentation of von Hippel-Lindau disease in a Chinese family.Q53311772
P433issue3
P407language of work or nameEnglishQ1860
P921main subjectvon Hippel-Lindau diseaseQ741315
P304page(s)675.e1-5
P577publication date2014-03-01
P1433published inUrologyQ7900884
P1476titleHigher prevalence of novel mutations in VHL gene in Chinese Von Hippel-Lindau disease patients.
P478volume83

Reverse relations

cites work (P2860)
Q47362904Genotype phenotype correlation in Asian Indian von Hippel-Lindau (VHL) syndrome patients with pheochromocytoma/paraganglioma
Q41754374Genotype-phenotype analysis of von Hippel-Lindau syndrome in fifteen Indian families.
Q38964723Profilin1 biology and its mutation, actin(g) in disease

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