Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: 1H NMR spectroscopy and genetic testing

Fig. 1

500 MHz 1H spectra of the urine of the two patients with FOS (b and c) and of a healthy subject (a). Assignments are as follows: 1 = trimethylamine-N-oxide (TMAO): 3.27 ppm; 2 = creatinine (Cr): 3.06 ppm; 3 = creatine (Cn): 3.04 ppm; 4 = trimethylamine (TMA): 2.92 ppm; 5 = dimethylamine (DMA): 2.73 ppm; 6 = citrate (cit): 2.56 and 2.72 ppm

Back to article page

Orphanet Journal of Rare Diseases

ISSN: 1750-1172