Article info
PDFElectronic letters
Comorbid VHL and SCA2 mutations in a large kindred: confounding diagnosis of neurological dysfunction caused by CNS VHL vascular tumours versus SCA2 atrophic neurodegeneration
- Correspondence to: Dr G M Glenn, Division of Cancer Epidemiology and Genetics, NCI/NIH/EPS/Room 7108, 6120 Executive Boulevard, MSC 7236, Bethesda, MD 20892-7236, USA; glenng{at}nih.gov
Citation
Comorbid VHL and SCA2 mutations in a large kindred: confounding diagnosis of neurological dysfunction caused by CNS VHL vascular tumours versus SCA2 atrophic neurodegeneration
Publication history
- First published July 1, 2002.
Online issue publication
April 27, 2016
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Copyright 2002 Journal of Medical Genetics