Case Report: Homozygous mutation in the ACAD9 gene revealed in a pediatric patient initially diagnosed with familial cardiac hypertrophy.

Kotlukova N, Kadykova A, Gorelova T, Dzik L, Islanov I, Zaklyazminskaya E

DOI: 10.3389/fmed.2026.1824617
Published: 2026
Container: Frontiers in medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fmed.2026.1824617,
  title = {Case Report: Homozygous mutation in the ACAD9 gene revealed in a pediatric patient initially diagnosed with familial cardiac hypertrophy.},
  author = {Kotlukova N and Kadykova A and Gorelova T and Dzik L and Islanov I and Zaklyazminskaya E},
  year = {2026},
  journal = {Frontiers in medicine},
  doi = {10.3389/fmed.2026.1824617},
  url = {https://doi.org/10.3389/fmed.2026.1824617}
}

RIS

TY  - JOUR
TI  - Case Report: Homozygous mutation in the ACAD9 gene revealed in a pediatric patient initially diagnosed with familial cardiac hypertrophy.
AU  - Kotlukova N
AU  - Kadykova A
AU  - Gorelova T
AU  - Dzik L
AU  - Islanov I
AU  - Zaklyazminskaya E
PY  - 2026
JO  - Frontiers in medicine
DO  - 10.3389/fmed.2026.1824617
UR  - https://doi.org/10.3389/fmed.2026.1824617
ER  -

APA

N, K., A, K., T, G., L, D., I, I., & E, Z. (2026). Case Report: Homozygous mutation in the ACAD9 gene revealed in a pediatric patient initially diagnosed with familial cardiac hypertrophy.. Frontiers in medicine. https://doi.org/10.3389/fmed.2026.1824617

Source records

pubmed · retrieved 2026-09-25T20:58:23.978Z