Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2
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S. Züchner | M. Lek | F. Muntoni | A. Mégarbané | Michael A. Gonzalez | R. Horvath | J. Christodoulou | S. Brandner | H. Houlden | S. Rahman | S. Scherer | Alexander J Abrams | P. Clayton | A. Pandraud | M. Reilly | M. Scoto | A. Manzur | Jean-Pierre Lin | A. Broomfield | A. Yonezawa | K. Matsubara | M. Menezes | M. King | Min Wang | M. Prasad | H. Jungbluth | V. Straub | J. Burns | R. Ouvrier | M. McGarvey | A. Foley | I. Hargreaves | P. Baxter | M. Farrell | K. Carpenter | W. Gold | J. Antony | I. Hughes | M. Lim | J. Land | A. H. Shah | R. Webster | J. O'Byrne | R. Phadke | S. Olpin | J. Ng | J. Urtizberea | K. O’Brien | B. McCullagh | E. Forman | Kumiko Sugano | A. Al-Odaib | Marcus Oppenheim | A. A. Mathew | J. O’Byrne | A. Mathew | K. O'Brien
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