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Molecular Genetics and Metabolism Reports logoLink to Molecular Genetics and Metabolism Reports
. 2022 Dec 7;34:100945. doi: 10.1016/j.ymgmr.2022.100945

Corrigendum to “ Biochemical diagnosis of aromatic-L-amino acid decarboxylase deficiency (AADCD) by assay of AADC activity in plasma using liquid chromatography/tandem mass spectrometry” [32/100888 (2022) page 1–4].

Gabriel Civallero a,b,⁎, Francyne Kubaski a,c, Danilo Pereira d,e, Gabriel Rübensam f, Zackary M Herbst g, Camilo Silva d, Franciele B Trapp a, Edina Poletto a,c, Larissa Faqueti a, Gabrielle Iop a, Juliano Soares a, Vanessa van der Linden h, Helio van der Linden h, Charles M Lourenço i, Roberto Giugliani a,b,j,k,l
PMCID: PMC9979259  PMID: 36873249

The authors would like to apologize for any inconvenience caused. (See Table 1.)

Table 1.

Clinical signs and genotype of the AADCD patients studied.

Patient number Gender Age (years) Genotype
1 Female 3.8 p.Arg347Gln/Trp121Arg
2 Male 3 p.Ser147Ile/Val60Ala
3 Male 10.1 p.Arg347Gln/Arg347Gln
4 Male 11.5 p.Arg347Gln/Arg347Gln
5 Male 2.7 p.Gln190Profs*13/p.Leu288Pro
6 Female 1.4 c.1040G > A (p.Arg347Gln) c.1055del (p.Pro352Hisfs*9)
7 Female 4.7 c.1040G > A; p.Arg347Gln

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