MNV-aware molecular characterization of a rare homozygous TTPA complex allele in ataxia with vitamin E deficiency.
- DOI
- 10.1007/s00438-026-02512-1
- Published
- 2026 Sep 9
- Container
- Molecular genetics and genomics : MGG
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s00438-026-02512-1,
title = {MNV-aware molecular characterization of a rare homozygous TTPA complex allele in ataxia with vitamin E deficiency.},
author = {Zaki-Dizaji M and Sarband MM},
year = {2026},
journal = {Molecular genetics and genomics : MGG},
doi = {10.1007/s00438-026-02512-1},
url = {https://doi.org/10.1007/s00438-026-02512-1}
}RIS
TY - JOUR TI - MNV-aware molecular characterization of a rare homozygous TTPA complex allele in ataxia with vitamin E deficiency. AU - Zaki-Dizaji M AU - Sarband MM PY - 2026 JO - Molecular genetics and genomics : MGG DO - 10.1007/s00438-026-02512-1 UR - https://doi.org/10.1007/s00438-026-02512-1 ER -
APA
M, Z., & MM, S. (2026). MNV-aware molecular characterization of a rare homozygous TTPA complex allele in ataxia with vitamin E deficiency.. Molecular genetics and genomics : MGG. https://doi.org/10.1007/s00438-026-02512-1
Source records
- pubmed · retrieved 2026-09-26T23:13:07.348Z