Associated Papers
Clinical and molecular characterization of an extended family with Fabry disease.
Wattanasirichaigoon D et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet, 2006
Fabry disease: identification of 50 novel alpha-galactosidase A mutations causing the classic phenotype and three-dimensional structural analysis of 29 missense mutations.
Shabbeer J et al.
Human Genomics, 2006
Select a paper to view details