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#616095 - MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY; MCT1D
Cytogenetic locations: ATP5PB
Gene summaries Genetic tests Medical literature
#610021 - HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 7; HHF7
Cytogenetic locations: ATP
*600682 - SOLUTE CARRIER FAMILY 16 (MONOCARBOXYLIC ACID TRANSPORTER), MEMBER 1; SLC16A1
#245340 - ERYTHROCYTE LACTATE TRANSPORTER DEFECT
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