Fabry disease: Comparison of enzymatic, linkage, and mutation analysis for carrier detection in a family with a novel mutation (30delG)
Ashton-Prolla, P., Ashley, G.A., Giugliani, R., Pires, R.F., Desnick, R.J., Eng, C.M.Volume:
84
Language:
english
Pages:
5
Journal:
American Journal of Medical Genetics
DOI:
10.1002/(sici)1096-8628(19990611)84:53.0.co;2-z
Date:
June, 1999
File:
PDF, 273 KB
english, 1999