LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea,spherophakia, and secondary glaucoma

D?(c)sir J, Sznajer Y, Depasse F, Roulez F, Schrooyen M, Meire F, Abramowicz M. LTBP2 null mutations in an autosomal recessive ocular syndrome with megalocornea,spherophakia, and secondary glaucoma. Eur J Hum Genet. 2010 Jul;18(7):761-7.