Wowra, B.; Wysocka-Kosmulska, M.; Stanienda-Sokół, K.; Łach-Wojnarowicz, O.; Dobrowolski, D.; Wylęgała, E.
Diagnostic Challenges of Axenfeld-Rieger Syndrome and a Novel FOXC1 Gene Mutation in a Polish Family. J. Clin. Med. 2024, 13, 5761.
https://doi.org/10.3390/jcm13195761
AMA Style
Wowra B, Wysocka-Kosmulska M, Stanienda-Sokół K, Łach-Wojnarowicz O, Dobrowolski D, Wylęgała E.
Diagnostic Challenges of Axenfeld-Rieger Syndrome and a Novel FOXC1 Gene Mutation in a Polish Family. Journal of Clinical Medicine. 2024; 13(19):5761.
https://doi.org/10.3390/jcm13195761
Chicago/Turabian Style
Wowra, Bogumił, Marzena Wysocka-Kosmulska, Karolina Stanienda-Sokół, Olga Łach-Wojnarowicz, Dariusz Dobrowolski, and Edward Wylęgała.
2024. "Diagnostic Challenges of Axenfeld-Rieger Syndrome and a Novel FOXC1 Gene Mutation in a Polish Family" Journal of Clinical Medicine 13, no. 19: 5761.
https://doi.org/10.3390/jcm13195761
APA Style
Wowra, B., Wysocka-Kosmulska, M., Stanienda-Sokół, K., Łach-Wojnarowicz, O., Dobrowolski, D., & Wylęgała, E.
(2024). Diagnostic Challenges of Axenfeld-Rieger Syndrome and a Novel FOXC1 Gene Mutation in a Polish Family. Journal of Clinical Medicine, 13(19), 5761.
https://doi.org/10.3390/jcm13195761
