A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein‐truncating variant
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V. Mootha | S. Calvo | J. Christodoulou | B. Morar | A. Compton | L. E. Formosa | N. Lake | M. Ryan | D. Stroud | D. Thorburn | P. Procopis