Author:
Khokhar S,Pillay G,Sen S,Agarwal E
Publisher
Springer Science and Business Media LLC
Reference36 articles.
1. Ben Yahia S, Ouechtati F, Jelliti B, Nouira S, Chakroun S, Abdelhak S et al. Clinical and genetic investigation of isolated microspherophakia in a consanguineous Tunisian family. J Hum Genet 2009; 54: 550–553.
2. Nelson LB, Maumenee IH . Ectopia lentis. Surv Ophthlamol 1982; 27: 143–160.
3. Kumar A, Duvvari MR, Prabhakaran VC, Shetty JS, Murthy GJ, Blanton SH . A homozygous mutation in LTBP2 causes isolated microspherophakia. Hum Genet 2010; 128: 365–371.
4. Desir J, Sznajer Y, Depasse F, Roulez F, Schrooyen M, Meire F et al. LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea, spherophakia, and secondary glaucoma. Europ. J Hum Genet 2010; 18: 761–767.
5. Khan AO, Aldahmesh MA, Alkuraya FS . Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma—a distinct phenotype caused by recessive LTBP2 mutations. Mol Vis 2011; 17: 2570–2579.
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