Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families.

Kotalevskaya YY, Stepanov VA

Open source

DOI: 10.3389/fmed.2024.1418239
Published: 2024
Container: Frontiers in medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fmed.2024.1418239,
  title = {Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families.},
  author = {Kotalevskaya YY and Stepanov VA},
  year = {2024},
  journal = {Frontiers in medicine},
  doi = {10.3389/fmed.2024.1418239},
  url = {https://doi.org/10.3389/fmed.2024.1418239}
}

RIS

TY  - JOUR
TI  - Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families.
AU  - Kotalevskaya YY
AU  - Stepanov VA
PY  - 2024
JO  - Frontiers in medicine
DO  - 10.3389/fmed.2024.1418239
UR  - https://doi.org/10.3389/fmed.2024.1418239
ER  -

APA

YY, K., & VA, S. (2024). Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families.. Frontiers in medicine. https://doi.org/10.3389/fmed.2024.1418239

Source records

pubmed · retrieved 2026-09-27T06:59:53.714Z
europe-pmc · retrieved 2026-09-27T06:59:53.711Z
doaj · retrieved 2026-09-27T06:59:53.749Z