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Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome

Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a9afbb0898234bdbb73155ac3de578b8

Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome

About this item

Full title

Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome

Publisher

London: BioMed Central

Journal title

Ai zheng, 2016-08, Vol.35 (9), p.441-446, Article 79

Language

English

Formats

Publication information

Publisher

London: BioMed Central

More information

Scope and Contents

Contents

Background: Von Hippel–Lindau(VHL) syndrome is a dominantly inherited multisystem cancer syndrome caused by a heterozygous mutation in the VHL tumor suppressor gene. Previous studies suggested that similar populations of Caucasian and Japanese patients have similar genotype or phenotype characteristics. In this comprehensive study of East Asian pat...

Alternative Titles

Full title

Clinical and molecular characteristics of East Asian patients with von Hippel–Lindau syndrome

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_a9afbb0898234bdbb73155ac3de578b8

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_a9afbb0898234bdbb73155ac3de578b8

Other Identifiers

ISSN

1000-467X,2523-3548,1944-446X

E-ISSN

1944-446X,2523-3548

DOI

10.1186/s40880-016-0141-z

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