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Page 1
Autosomal recessive congenital hereditary corneal dystrophy associated with a novel SLC4A11 mutation in two consanguineous Tunisian families.
Br J Ophthalmol. 2022 Feb;106(2):281-287. doi: 10.1136/bjophthalmol-2020-318204. Epub 2021 Apr 20.
Br J Ophthalmol. 2022.
PMID: 33879471
A novel missense mutation in the ESRRB gene causes DFNB35 hearing loss in a Tunisian family.
Ben Saïd M, Ayedi L, Mnejja M, Hakim B, Khalfallah A, Charfeddine I, Khifagi C, Turki K, Ayadi H, Benzina Z, Ghorbel A, Castillo ID, Masmoudi S, Aifa MH.
Ben Saïd M, et al. Among authors: aifa mh.
Eur J Med Genet. 2011 Nov-Dec;54(6):e535-41. doi: 10.1016/j.ejmg.2011.06.008. Epub 2011 Jul 13.
Eur J Med Genet. 2011.
PMID: 21802533
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