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Mutations in known disease genes account for the majority of autosomal recessive retinal dystrophies.
Patel N, Alkuraya H, Alzahrani SS, Nowailaty SR, Seidahmed MZ, Alhemidan A, Ben-Omran T, Ghazi NG, Al-Aqeel A, Al-Owain M, Alzaidan HI, Faqeih E, Kurdi W, Rahbeeni Z, Ibrahim N, Abdulwahab F, Hashem M, Shaheen R, Abouelhoda M, Monies D, Khan AO, Aldahmesh MA, Alkuraya FS. Patel N, et al. Clin Genet. 2018 Dec;94(6):554-563. doi: 10.1111/cge.13426. Epub 2018 Sep 3. Clin Genet. 2018. PMID: 30054919
Fibrocartilaginous embolism: a rare cause of cervical spine infarction.
Abu Mayyala W, Abu Aqeel N, Jobran AWM, Shaheen F, Abdulrazzak M, Alhroub Y. Abu Mayyala W, et al. Ann Med Surg (Lond). 2024 Apr 4;86(5):3165-3168. doi: 10.1097/MS9.0000000000002005. eCollection 2024 May. Ann Med Surg (Lond). 2024. PMID: 38694385 Free PMC article.