Comments on 'Infantile hypophosphatasia without bone deformities presenting with severe pyridoxine-resistant seizures' in Molecular Genetics and Metabolism' 2014 Mar;111(3):404-7 by M.G. de Roo, N.G. Abeling, C.B. Majoie, A.M. Bosch, J.H. Koelman, J.M. Cobben, M. Duran, B.T. Poll-The.

van der Stoep, Nienke; Onkenhout, Willem; Prins, Sandra; Struys, Eduard; Jakobs, Cornelis; Peeters-Scholte, Cacha

van der Stoep, Nienke; Onkenhout, Willem; Prins, Sandra; Struys, Eduard; Jakobs, Cornelis; Peeters-Scholte, Cacha.

Afiliação

van der Stoep N; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Onkenhout W; Department of Clinical Chemistry and Laboratory Medicine, Unit of Metabolic Diseases, Leiden University Medical Center, Leiden, The Netherlands.
Prins S; Department of Neonatology, Leiden University Medical Center, Leiden, The Netherlands.
Struys E; Metabolic Unit and Department of Clinical Chemistry, VU University Medical Center, Amsterdam, The Netherlands.
Jakobs C; Metabolic Unit and Department of Clinical Chemistry, VU University Medical Center, Amsterdam, The Netherlands.
Peeters-Scholte C; Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.

Mol Genet Metab Rep ; 1: 220-222, 2014.

Article em En | MEDLINE | ID: mdl-27896090