Heterozygous deep-intronic variants and deletions in ABCA4 in persons with retinal dystrophies and one exonic ABCA4 variant

MLA

Bax, N. M., et al. “Heterozygous Deep-Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant.” Human Mutation, 2015. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1284107087&authtype=sso&custid=ns315887.

APA

Bax, N. M., Sangermano, R., Roosing, S., Thiadens, A. A. H. J., Hoefsloot, L. H., Born, L. I. van den, Phan, M., Klevering, B. J., Westeneng-van Haaften, S. C., Braun, T. A., Zonneveld-Vrieling, M. N., Wijs, I. de, Mutlu, M., Stone, E. M., Hollander, A. I. den, Klaver, C. C., Hoyng, C. B., & Cremers, F. P. M. (2015). Heterozygous deep-intronic variants and deletions in ABCA4 in persons with retinal dystrophies and one exonic ABCA4 variant. Human Mutation.

Chicago

Bax, N.M., R. Sangermano, S. Roosing, A.A.H.J. Thiadens, L.H. Hoefsloot, L.I. van den Born, M. Phan, et al. 2015. “Heterozygous Deep-Intronic Variants and Deletions in ABCA4 in Persons with Retinal Dystrophies and One Exonic ABCA4 Variant.” Human Mutation. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsoai&AN=edsoai.on1284107087&authtype=sso&custid=ns315887.