HADHHydroxyacyl-Coenzyme A Dehydrogenase (biochemistry)
HADHHorse Liver Alcohol Dehydrogenase
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The HADH mutation is inherited in an autosomal recessive pattern and has been reported in 3 families (32).
2] Human genes: ABCC8, ATP-binding cassette subfamily C, member 8; KCNJ11, potassium inwardly rectifying channel, subfamily J, member 11; GCK, glucokinase; GLUD1, glutamate dehydrogenase 1; HADH, hydroxyacyl-Coenzyme A dehydrogenase; SLC16A1, solute carrier family 16, member 1 (monocarboxylic acid transporter 1).
ATP]-HI ABCC8 11p15 AD KCNJ11 GDH-HI (HI/HA) GLUD-1 10q AD GK-HI GCK 7p AD SCHAD-HI HADH 4q AR MCT1 (EIHI) SLC16A1 1p AD Genetic form Clinical features [K.