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Description
Rohrmann S, Linseisen J, Allenspach M, von Eckardstein A, Mller D
ACIDIFIER: CITRIC ACID
Rare mutations in the SLC22A5 gene can cause a genetic condition called primary carnitine deficiency, which is usually discovered in infancy because it affects brain function, muscle function, and blood glucose levels
[DOI] [PMC free article] [PubMed] [Google Scholar] 164.Tamai I
