Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients (Q28261894)

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Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients
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    Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients (English)
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    F Taroni
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    E Verderio
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    F Dworzak
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    P J Willems
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    P Cavadini
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    S DiDonato
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    July 1993
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    4
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    314-20
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    3
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