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Mutations in DDHD2, encoding an intracellular phospholipase A1, cause a recessive form of complex hereditary spastic paraplegia
American Journal of Physiology, 1993
Surprisingly, unlike C@PA(+), SeC@PA(+) exhibited the highest RS levels in 8 mM GSH solution, which was attributed to Se producing RS with more oxidative activity by decomposing GSH
time 97 (n) 93 (n) ICU patients Panahi (RCT) 1% 0.99 [0.94-1.05] hosp
Longitudinal monitoring can identify suspicious patterns even when specific peptide tests are negative
