GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia
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J. Berg | K. Wilhelmsen | Zheng Fan | Y. Shiloh-Malawsky | M. Tennison | K. Crooks | M. Roche | K. Weck | R. Greenwood | J. Evans | Ana C. G. Felix | Ana Felix
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