Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency

Olimpia Musumeci, Mohammed Aguennouz, Giacomo Pietro Comi, Carmelo Rodolico, Massimo Autunno, Andreina Bordoni, Silvia Baratta, Franco Taroni, Giuseppe Vita, Antonio Toscano

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Medicine & Life Sciences