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Description
First Case Report of Primary Carnitine Deficiency Manifested as Intellectual Disability and Autism Spectrum Disorder
doi: 10.1177/1941406409342121
Janmey PA et al (2013) From tissue mechanics to transcription factors
10.1007/s00125-012-2469-5 171 PiconeP.DittaL
The former is characterized by impairment of expression of tyrosine, tyrosine hydroxylase (TH), DAT, and serotonin transporters (SERT), as well as DA depletion, decrease in the density of DA D2 receptors, hypo-dopaminergic status, and neuronal degeneration (Wilson et al
coli s SHMT GlyA, which shares 48% amino acid identity with the N
