Bibliographic Details
| Title: |
Diagnostic dilemma: A young woman with Fabry disease symptoms, no family history, and a “sequencing cryptic” α-galactosidase a large deletion |
| Authors: |
Feldt-Rasmussen, Ulla1 ufeldt@rh.dk, Dobrovolny, Robert2, Nazarenko, Irina2, Ballegaard, Martin3, Hasholt, Lis4, Rasmussen, Åse K.1, Christensen, Erik I.5, Sorensen, Soren S.6, Wibrand, Flemming7, Desnick, Robert J.2 robert.desnick@mssm.edu |
| Source: |
Molecular Genetics & Metabolism. Nov2011, Vol. 104 Issue 3, p314-318. 5p. |
| Database: |
Academic Search Ultimate |
