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Nonsense and frameshift mutations, however, are typically associated with lower carnitine transport and are more prevalent in symptomatic individuals, whereas missense mutations and in-frame deletions (with some residual carnitine transport activity) are more prevalent in asymptomatic mothers identified by newborn screening of their unaffected infants [82]
Jiminez JA, et al
Siliprandi N, Di Lisa F, Menabo R (1990) Clinical use of carnitine
As has been previously discussed, NO is felt to possess inherent anti-fibrotic properties
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