A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients (Q44120180)

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scientific article published in September 2002
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A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients
scientific article published in September 2002

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    A founder mutation (R254X) of SLC22A5 (OCTN2) in Chinese primary carnitine deficiency patients (English)

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