EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia.
- DOI
- 10.1016/j.ejmg.2022.104574
- Published
- 2022 Oct
- Container
- European journal of medical genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.ejmg.2022.104574,
title = {EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia.},
author = {Courdier C and Gemahling A and Guindolet D and Barjol A and Scaramouche C and Bouneau L and Calvas P and Martin G and Chassaing N and Plaisancié J},
year = {2022},
journal = {European journal of medical genetics},
doi = {10.1016/j.ejmg.2022.104574},
url = {https://doi.org/10.1016/j.ejmg.2022.104574}
}RIS
TY - JOUR TI - EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia. AU - Courdier C AU - Gemahling A AU - Guindolet D AU - Barjol A AU - Scaramouche C AU - Bouneau L AU - Calvas P AU - Martin G AU - Chassaing N AU - Plaisancié J PY - 2022 JO - European journal of medical genetics DO - 10.1016/j.ejmg.2022.104574 UR - https://doi.org/10.1016/j.ejmg.2022.104574 ER -
APA
C, C., A, G., D, G., A, B., C, S., L, B., P, C., G, M., N, C., & J, P. (2022). EPHA2 biallelic disruption causes syndromic complex microphthalmia with iris hypoplasia.. European journal of medical genetics. https://doi.org/10.1016/j.ejmg.2022.104574
Source records
- pubmed · retrieved 2026-11-10T11:17:49.605Z