Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy.

Mohammadi M, Rahimoghli M, Ghasemi A, Okhovat AA, Alavi A

DOI: 10.1038/s10038-026-01467-w
Published: 2026 Jul
Container: Journal of human genetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1038/s10038-026-01467-w,
  title = {Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy.},
  author = {Mohammadi M and Rahimoghli M and Ghasemi A and Okhovat AA and Alavi A},
  year = {2026},
  journal = {Journal of human genetics},
  doi = {10.1038/s10038-026-01467-w},
  url = {https://doi.org/10.1038/s10038-026-01467-w}
}

RIS

TY  - JOUR
TI  - Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy.
AU  - Mohammadi M
AU  - Rahimoghli M
AU  - Ghasemi A
AU  - Okhovat AA
AU  - Alavi A
PY  - 2026
JO  - Journal of human genetics
DO  - 10.1038/s10038-026-01467-w
UR  - https://doi.org/10.1038/s10038-026-01467-w
ER  -

APA

M, M., M, R., A, G., AA, O., & A, A. (2026). Expanding the phenotypic spectrum of LAMA2-related disorders: Axonal neuropathy in the absence of muscular dystrophy.. Journal of human genetics. https://doi.org/10.1038/s10038-026-01467-w

Source records

pubmed · retrieved 2026-09-26T11:47:15.449Z