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Carrier Frequency of a Common Mutation of Carnitine Palmitoyltransferase 1A Deficiency and Long-Term Follow-Up in Finland

✍ Scribed by Eva Roomets; Padmini P. Polinati; Liliya Euro; Petra M. Eskelin; Aila Paganus; Tiina Tyni

No coin nor oath required. For personal study only.

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