Tyrosine Hydroxylase Deficiency: Studies in patient samples and in a cellular model 

Tristán Noguero, Alba (Data de defensa: 2019-11-22)

Monoamine Neurotransmitter diseases are a rare group of inherited disorders of metabolism that encompass 12 different genetic defects leading to abnormal dopamine and/or serotonin brain homeostasis. They correspond to ...