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Wu D et al (2023): Transport and inhibition mechanisms of human VMAT2

Thus, given these findings, it would be logical to suggest that the mGSH pool may be a good choice as a therapeutic target

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Prader-Willi syndrome appears through loss of the paternal allele of chromosome 15q11-q13 [8 ]and it is characterized by hypotonia in infants, followed by obesity and excessive eating after early childhood, associated with significant mental impairments [12, 58]

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