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Angius A, Uva P, Buers I, et al. Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. Am J Hum Genet. 2018;102(4):713doi: 10.1016/j.ajhg.2018.03.020.
Angius, A., Uva, P., Buers, I., Oppo, M., Puddu, A., Onano, S., Persico, I., Loi, A., Marcia, L., Höhne, W., Cuccuru, G., Fotia, G., Deiana, M., Marongiu, M., Atalay, H. T., Inan, S., El Assy, O., Smit, L. M. E., Okur, I., Boduroglu, K., Utine, G. E., Kılıç, E., Zampino, G., Crisponi, G., Crisponi, L., & Rutsch, F. (2018). Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. American journal of human genetics, 102(4), 713. https://doi.org/10.1016/j.ajhg.2018.03.020
Angius, Andrea, et al. "Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa." American journal of human genetics vol. 102,4 (2018): 713. doi: https://doi.org/10.1016/j.ajhg.2018.03.020
Angius A, Uva P, Buers I, Oppo M, Puddu A, Onano S, Persico I, Loi A, Marcia L, Höhne W, Cuccuru G, Fotia G, Deiana M, Marongiu M, Atalay HT, Inan S, El Assy O, Smit LME, Okur I, Boduroglu K, Utine GE, Kılıç E, Zampino G, Crisponi G, Crisponi L, Rutsch F. Bi-allelic Mutations in KLHL7 Cause a Crisponi/CISS1-like Phenotype Associated with Early-Onset Retinitis Pigmentosa. Am J Hum Genet. 2018 Apr 05;102(4):713. doi: 10.1016/j.ajhg.2018.03.020. PMID: 29625027; PMCID: PMC5985354.
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