Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency.

Babiker MOE, Kurian MA, Suleiman J

DOI: 10.3389/fped.2022.964201
Published: 2022
Container: Frontiers in pediatrics
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fped.2022.964201,
  title = {Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency.},
  author = {Babiker MOE and Kurian MA and Suleiman J},
  year = {2022},
  journal = {Frontiers in pediatrics},
  doi = {10.3389/fped.2022.964201},
  url = {https://doi.org/10.3389/fped.2022.964201}
}

RIS

TY  - JOUR
TI  - Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency.
AU  - Babiker MOE
AU  - Kurian MA
AU  - Suleiman J
PY  - 2022
JO  - Frontiers in pediatrics
DO  - 10.3389/fped.2022.964201
UR  - https://doi.org/10.3389/fped.2022.964201
ER  -

APA

MOE, B., MA, K., & J, S. (2022). Case report: First case report of an Emirati child with a novel gene variant causing aromatic L-amino acid decarboxylase deficiency.. Frontiers in pediatrics. https://doi.org/10.3389/fped.2022.964201

Source records

pubmed · retrieved 2026-11-10T12:49:06.519Z
europe-pmc · retrieved 2026-11-10T12:49:06.529Z