LTBP2gene analysis in theGLC3C-linked family and 94CYP1B1-negative cases with primary congenital glaucoma

Genetics of primary glaucoma

(2011) Arif O. Khan   CURRENT OPINION IN OPHTHALMOLOGY

Molecular Characterization of Newborn Glaucoma Including a Distinct Aniridic Phenotype

(2011) Arif O. Khan et al.   OPHTHALMIC GENETICS

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

(2010) Julie Désir et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A homozygous mutation in LTBP2 causes isolated microspherophakia

(2010) Arun Kumar et al.   HUMAN GENETICS

Null Mutations in LTBP2 Cause Primary Congenital Glaucoma

(2009) Manir Ali et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Visual impairment secondary to congenital glaucoma in children: visual responses, optical correction and use of low vision AIDS

(2009) Maria Aparecida Onuki Haddad et al.   Clinics

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

(2009) Mehrnaz Narooie-Nejad et al.   HUMAN MOLECULAR GENETICS

CYP1B1 and MYOC Mutations in 116 Chinese Patients With Primary Congenital Glaucoma

(2008) Yuhong Chen   ARCHIVES OF OPHTHALMOLOGY