Mansilla, P. F., Lima, V. L., Salomão, G. H. A., & Christofolini, D. M. (2024). Genetic Variants in Rare Ophthalmological Syndromes: Novel COL11A1 Splice Site Variant in a Brazilian Family with Stickler Syndrome Type 2. Wolters Kluwer Medknow Publications.
Chicago Style (17th ed.) CitationMansilla, Pedro Filipecki, Vagner Loduca Lima, Gustavo Henrique Araújo Salomão, and Denise Maria Christofolini. Genetic Variants in Rare Ophthalmological Syndromes: Novel COL11A1 Splice Site Variant in a Brazilian Family with Stickler Syndrome Type 2. Wolters Kluwer Medknow Publications, 2024.
MLA (9th ed.) CitationMansilla, Pedro Filipecki, et al. Genetic Variants in Rare Ophthalmological Syndromes: Novel COL11A1 Splice Site Variant in a Brazilian Family with Stickler Syndrome Type 2. Wolters Kluwer Medknow Publications, 2024.