Detection of three families with GLA p.A143T mutation and low α-galactosidase levels by newborn screening for Fabry disease

Samantha A Marcellus, Myrl D. Holida, John A. Bernat
  • Molecular Genetics and Metabolism, January 2017, Elsevier
  • DOI: 10.1016/j.ymgme.2016.11.224

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The following have contributed to this page: Mr Myrl D. Holida