Novel missense mutation (Arg432Cys) in a patient with steroid sulphatase-deficiency
L. M. González-Huerta,
M. R. Riviera-Vega,
S. H. Kofman-Alfeuro,
S. A. Cuevas-Covarrubias,
L. M. González-Huerta
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorM. R. Riviera-Vega
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorS. H. Kofman-Alfeuro
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorS. A. Cuevas-Covarrubias
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorL. M. González-Huerta,
M. R. Riviera-Vega,
S. H. Kofman-Alfeuro,
S. A. Cuevas-Covarrubias,
L. M. González-Huerta
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorM. R. Riviera-Vega
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorS. H. Kofman-Alfeuro
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this authorS. A. Cuevas-Covarrubias
Serriciode Genetica, Hospital General de Mexico, facultad de Medicina, UNAM & México D.F., México.
Search for more papers by this author
References
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