Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.
- DOI
- 10.1016/j.gmg.2026.100098
- Published
- 2026 Sep
- Container
- Global medical genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.gmg.2026.100098,
title = {Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.},
author = {Rojas-Morales E and Esparza-García E and Magaña-Torres MT},
year = {2026},
journal = {Global medical genetics},
doi = {10.1016/j.gmg.2026.100098},
url = {https://doi.org/10.1016/j.gmg.2026.100098}
}RIS
TY - JOUR TI - Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review. AU - Rojas-Morales E AU - Esparza-García E AU - Magaña-Torres MT PY - 2026 JO - Global medical genetics DO - 10.1016/j.gmg.2026.100098 UR - https://doi.org/10.1016/j.gmg.2026.100098 ER -
APA
E, R., E, E., & MT, M. (2026). Clinical and molecular characterization of giant axonal neuropathy due to a homozygous c.851 + 1G>A variant in GAN: A case report and literature review.. Global medical genetics. https://doi.org/10.1016/j.gmg.2026.100098
Source records
- pubmed · retrieved 2026-09-25T16:47:12.654Z
- europe-pmc · retrieved 2026-09-25T16:47:12.678Z