Clinical and biochemical footprints of inherited disorders of heme synthesis and porphyrias: Insights from the IEMbase and dyadic nomenclature.
- DOI
- 10.1016/j.ymgme.2026.110292
- Published
- 2026-10-17
- Container
- Mol Genet Metab
- Publisher
- Not recorded
- Open access
- no
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Cite this work
BibTeX
@article{allodium:10.1016/j.ymgme.2026.110292,
title = {Clinical and biochemical footprints of inherited disorders of heme synthesis and porphyrias: Insights from the IEMbase and dyadic nomenclature.},
author = {Barman-Aksözen J and Ferreira CR and Blau N.},
year = {2026},
journal = {Mol Genet Metab},
doi = {10.1016/j.ymgme.2026.110292},
url = {https://doi.org/10.1016/j.ymgme.2026.110292}
}RIS
TY - JOUR TI - Clinical and biochemical footprints of inherited disorders of heme synthesis and porphyrias: Insights from the IEMbase and dyadic nomenclature. AU - Barman-Aksözen J AU - Ferreira CR AU - Blau N. PY - 2026 JO - Mol Genet Metab DO - 10.1016/j.ymgme.2026.110292 UR - https://doi.org/10.1016/j.ymgme.2026.110292 ER -
APA
J, B., CR, F., & N., B. (2026). Clinical and biochemical footprints of inherited disorders of heme synthesis and porphyrias: Insights from the IEMbase and dyadic nomenclature.. Mol Genet Metab. https://doi.org/10.1016/j.ymgme.2026.110292
Source records
- europe-pmc · retrieved 2026-11-10T13:24:30.482Z