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Improved Detection of Germline Mutations in Korean VHL Patients by Multiple Ligation-dependent Probe Amplification Analysis

von Hippel-Lindau (VHL) disease is an autosomal dominant inherited tumor syndrome characterized by the development of tumors in the eye, brain, spinal cord, inner ear, adrenal gland, pancreas, kidney, and epididymis, associated with germline mutations in the VHL gene. We used sequentially sequencing...

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Bibliografiske detaljer
Main Authors: Cho, Hyun-Jung, Ki, Chang-Seok, Kim, Jong-Won
Format: Artigo
Sprog:Inglês
Udgivet: The Korean Academy of Medical Sciences 2009
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2650969/
https://ncbi.nlm.nih.gov/pubmed/19270817
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2009.24.1.77
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