Genetic basis of clinical catecholamine disorders.

Garland EM, Hahn MK, Ketch TP, Keller NR, Kim CH, Kim KS, Biaggioni I, Shannon JR, Blakely RD, Robertson D
Ann N Y Acad Sci. 2002 971: 506-14

PMID: 12438171 · DOI:10.1111/j.1749-6632.2002.tb04515.x

MeSH Terms (14)

Catecholamines DNA, Complementary Dopamine Dopamine beta-Hydroxylase Exons Heterozygote Humans Models, Biological Models, Chemical Mutation Mutation, Missense Norepinephrine Plasma Membrane Transport Proteins Symporters Syndrome

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