Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.
- DOI
- 10.1038/s41598-020-65737-z
- Published
- 2020 Jun 12
- Container
- Scientific reports
- Publisher
- Not recorded
- Open access
- yes
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BibTeX
@article{allodium:10.1038/s41598-020-65737-z,
title = {Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.},
author = {Fujinami-Yokokawa Y and Fujinami K and Kuniyoshi K and Hayashi T and Ueno S and Mizota A and Shinoda K and Arno G and Pontikos N and Yang L and Liu X and Sakuramoto H and Katagiri S and Mizobuchi K and Kominami T and Terasaki H and Nakamura N and Kameya S and Yoshitake K and Miyake Y and Kurihara T and Tsubota K and Miyata H and Iwata T and Tsunoda K and Japan Eye Genetics Consortium},
year = {2020},
journal = {Scientific reports},
doi = {10.1038/s41598-020-65737-z},
url = {https://doi.org/10.1038/s41598-020-65737-z}
}RIS
TY - JOUR TI - Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association. AU - Fujinami-Yokokawa Y AU - Fujinami K AU - Kuniyoshi K AU - Hayashi T AU - Ueno S AU - Mizota A AU - Shinoda K AU - Arno G AU - Pontikos N AU - Yang L AU - Liu X AU - Sakuramoto H AU - Katagiri S AU - Mizobuchi K AU - Kominami T AU - Terasaki H AU - Nakamura N AU - Kameya S AU - Yoshitake K AU - Miyake Y AU - Kurihara T AU - Tsubota K AU - Miyata H AU - Iwata T AU - Tsunoda K AU - Japan Eye Genetics Consortium PY - 2020 JO - Scientific reports DO - 10.1038/s41598-020-65737-z UR - https://doi.org/10.1038/s41598-020-65737-z ER -
APA
Y, F., K, F., K, K., T, H., S, U., A, M., K, S., G, A., N, P., L, Y., X, L., H, S., S, K., K, M., T, K., H, T., N, N., S, K., K, Y., Y, M., T, K., K, T., H, M., T, I., K, T., & Consortium, J. E. G. (2020). Clinical and Genetic Characteristics of 18 Patients from 13 Japanese Families with CRX-associated retinal disorder: Identification of Genotype-phenotype Association.. Scientific reports. https://doi.org/10.1038/s41598-020-65737-z
Source records
- pubmed · retrieved 2026-09-27T12:09:15.938Z