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The most likely candidates among them may be -aminobutyraldehyde dehydrogenase PatD that is active with unmethylated TMABA (-aminobutyraldehyde) or with betaine aldehyde (Samsonova et al., 2005) and PuuC, a non-specific aldehyde dehydrogenase that oxidizes all aldehydes in putrescine catabolism including -aminobutyraldehyde (Schneider and Reitzer, 2012)
[DOI] [PubMed] [Google Scholar] 85.Ellaway C.J., Peat J., Williams K., Leonard H., Christodoulou J
The patient was found to have carnitine deficiency
The ACACB gene is located on chromosome 12q24.11 and is composed of 58 exons that encode a precursor protein of 2,458 amino acids
