UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

Increasing evidence that genetic variation in Complement factor H related 5 (CFHR5) causes disease: A commentary on 'Atypical haemolytic uremic syndrome and genetic aberrations in the complement factor-H-related 5 gene'

Maxwell, PH; (2012) Increasing evidence that genetic variation in Complement factor H related 5 (CFHR5) causes disease: A commentary on 'Atypical haemolytic uremic syndrome and genetic aberrations in the complement factor-H-related 5 gene'. JOURNAL OF HUMAN GENETICS , 57 (8) pp. 473-474. 10.1038/jhg.2012.80.

Full text not available from this repository.
Type: Article
Title: Increasing evidence that genetic variation in Complement factor H related 5 (CFHR5) causes disease: A commentary on 'Atypical haemolytic uremic syndrome and genetic aberrations in the complement factor-H-related 5 gene'
DOI: 10.1038/jhg.2012.80
Keywords: Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, GENETICS & HEREDITY, GLOMERULONEPHRITIS
UCL classification: UCL > School of Life and Medical Sciences
UCL > School of Life and Medical Sciences > Faculty of Medical Sciences
URI: http://discovery.ucl.ac.uk/id/eprint/1362919
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item