Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations

Wenli Zhou, Veronica Marchesi, Matthew McLeod, Anna Jolanta Kordala, Sylwia Szwec, Julia Anna Mielcarz, Angelo Poletti, Barbara Tedesco

Open source

DOI
10.1016/j.bbadis.2026.168244
Published
2026-08
Container
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Publisher
Elsevier BV
Open access
unknown

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BibTeX

@article{allodium:10.1016/j.bbadis.2026.168244,
  title = {Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations},
  author = {Wenli Zhou and Veronica Marchesi and Matthew McLeod and Anna Jolanta Kordala and Sylwia Szwec and Julia Anna Mielcarz and Angelo Poletti and Barbara Tedesco},
  year = {2026},
  journal = {Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease},
  doi = {10.1016/j.bbadis.2026.168244},
  url = {https://doi.org/10.1016/j.bbadis.2026.168244}
}

RIS

TY  - JOUR
TI  - Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations
AU  - Wenli Zhou
AU  - Veronica Marchesi
AU  - Matthew McLeod
AU  - Anna Jolanta Kordala
AU  - Sylwia Szwec
AU  - Julia Anna Mielcarz
AU  - Angelo Poletti
AU  - Barbara Tedesco
PY  - 2026
JO  - Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
DO  - 10.1016/j.bbadis.2026.168244
UR  - https://doi.org/10.1016/j.bbadis.2026.168244
ER  - 

APA

Zhou, W., Marchesi, V., McLeod, M., Kordala, A. J., Szwec, S., Mielcarz, J. A., Poletti, A., & Tedesco, B. (2026). Molecular, cellular, and clinical aspects of myofibrillar myopathy caused by HSPB8 frameshift mutations. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. https://doi.org/10.1016/j.bbadis.2026.168244

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