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A novel mutation of the RRM2B gene in an infant with early fatal encephalomyopathy, central hypomyelination, and tubulopathy

✍ Scribed by Birgit Acham-Roschitz; Barbara Plecko; Franz Lindbichler; Reginald Bittner; Christoph J. Mache; Wolfgang Sperl; Johannes A. Mayr

No coin nor oath required. For personal study only.

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