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    Diagnosis of Primary Trimethylaminuria in an Affected Patient With a Rare Genotype in Sub‐Saharan Africa

    Diagnosis of Primary Trimethylaminuria in an Affected Patient With a Rare Genotype in Sub‐Saharan Africa by M. Dercksen, M. Perumal, E. Davoren, D. R. Reed, C. Murry‐Maritz, R. van derSluis, S. Mason

    Published 2025-03-01
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