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Cognitive dysfunction and hypogonadotrophic hypogonadism in a Brazilian patient with mitochondrial neurogastrointestinal encephalomyopathy and a novel ECGF1 mutation

✍ Scribed by F. J. Carod-Artal; M. D. Herrero; M. C. Lara; E. López-Gallardo; E. Ruiz-Pesini; R. Martí; J. Montoya

No coin nor oath required. For personal study only.

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