Expanding the clinical and molecular spectrum of thiamine pyrophosphokinase deficiency: a treatable neurological disorder caused by TPK1 mutations.
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H. Prokisch | W. Yue | S. Banka | T. Marquardt | W. Sperl | K. Chandler | O. Debus | C. Hart | J. Mayr | H. Sonwalkar | C. Makowski | C. de Goede | Nasaim Khan | F. Zimmermann | R. Feichtinger | A. Morris | K. Nosaka | Lavinija Mataković | Beate von Bremen | V. Lunzer