Gene List:
ABAT, ALDH5A1, ALDH7A1, AMT, ARHGEF9, ASNS, ATP1A3, CACNA1A, CACNA1B, CBS, CLTC, COMT, DBH, DDC, DHFR, DRD3, DRD4, DRD5, FOLR1, GABRA1, GABRB3, GABRD, GABRG2, GAD1, GCH1, GCSH, GLDC, GLRA1, GLRB, GLUL, GNAQ, GPHN, HTR1A, HTR2A, MAOA, MTHFD1, MTHFR, PC, PCBD1, PHGDH, PITX3, PNPO, PSAT1, PSPH, PTS, QDPR, SLC1A3, SLC25A22, SLC46A1, SLC6A1, SLC6A2, SLC6A3, SLC6A4, SLC6A5, SLC6A9, SNAP25, SNAP29, SNCA, SPR, STXBP1, SYN1, SYN2, SYP, TH, TPH2

References:
Pronicka E, et al New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre. J Transl Med. 2016 Jun 12;14(1):174.

Wen W, et al. NGS in argininosuccinic aciduria detects a mutation (D145G) which drives alternative splicing of ASL: a case report study. BMC Med Genet. 2016 Feb 3;17:9.