Monocarboxylate transporter 1 deficiency: a rare case report and systematic review of genetically confirmed cases.

Khalifa YM, Assem MY, Ahmed ZF, Hasan LT, Qutob IA

DOI: 10.1097/ms9.0000000000005477
Published: 2026 Sep
Container: Annals of medicine and surgery (2012)
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1097/ms9.0000000000005477,
  title = {Monocarboxylate transporter 1 deficiency: a rare case report and systematic review of genetically confirmed cases.},
  author = {Khalifa YM and Assem MY and Ahmed ZF and Hasan LT and Qutob IA},
  year = {2026},
  journal = {Annals of medicine and surgery (2012)},
  doi = {10.1097/ms9.0000000000005477},
  url = {https://doi.org/10.1097/ms9.0000000000005477}
}

RIS

TY  - JOUR
TI  - Monocarboxylate transporter 1 deficiency: a rare case report and systematic review of genetically confirmed cases.
AU  - Khalifa YM
AU  - Assem MY
AU  - Ahmed ZF
AU  - Hasan LT
AU  - Qutob IA
PY  - 2026
JO  - Annals of medicine and surgery (2012)
DO  - 10.1097/ms9.0000000000005477
UR  - https://doi.org/10.1097/ms9.0000000000005477
ER  -

APA

YM, K., MY, A., ZF, A., LT, H., & IA, Q. (2026). Monocarboxylate transporter 1 deficiency: a rare case report and systematic review of genetically confirmed cases.. Annals of medicine and surgery (2012). https://doi.org/10.1097/ms9.0000000000005477

Source records

pubmed · retrieved 2026-09-26T13:36:05.821Z