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Please use this identifier to cite or link to this item: https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/98
Title: Prostate cancer in a male with Holt-Oram Syndrome: First clinical association of the TBX5 mutation
Authors: Aherne, N. J.
Rangaswamy, G.
Thirion, P.
MNCLHD Author: Aherne, Noel J.
Issue Date: 2013
Citation: Case reports in urology. 2013:2013:405343. doi: 10.1155/2013/405343. Epub 2013 Aug 5.
Abstract: Holt-Oram syndrome is an autosomal dominant disorder which is caused by mutations of TBX5 and is characterised by cardiac and skeletal abnormalities. TBX5 is part of the T-box gene family and is thought to upregulate tumour cell proliferation and metastasis when mutated. We report the first clinical case of prostate cancer in an individual with Holt Oram syndrome.
URI: https://mnclhd.intersearch.com.au/mnclhdjspui/handle/123456789/98
Keywords: Holt-Oram Syndrome;Prostatic Neoplasms
Appears in Collections:Oncology / Cancer

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