Variations in the human Crumbs homolog-1 (CRB1) gene lead to an array of retinal
dystrophies including early onset of retinitis pigmentosa (RP) and Leber congenital …

Variations in the Crumbs homolog-1 (CRB1) gene are associated with a wide variety of
autosomal recessive retinal dystrophies, including early onset retinitis pigmentosa (RP) and …

Mutations in the human Crumbs homologue-1 (CRB1) gene cause retinal diseases
including Leber's congenital amaurosis (LCA) and retinitis pigmentosa type 12. The CRB1 …

In humans, the Crumbs homolog-1 (CRB1) gene is mutated in autosomal recessive Leber
congenital amaurosis and early-onset retinitis pigmentosa. In mammals, the Crumbs family …

The mammalian apical-basal determinant Crumbs homolog-1 (CRB1) plays a crucial role in
retinal structure and function by the maintenance of adherens junctions between …

Mutations in the human Crumbs homologue-1 (CRB1) gene cause retinal blinding diseases,
such as Leber congenital amaurosis and retinitis pigmentosa. In the previous studies we …

In humans, the Crumbs homolog-1 (CRB1) gene is mutated in progressive types of
autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. However, there …

Mutations in the Crumbs homologue 1 (CRB1) gene cause autosomal recessive retinitis
pigmentosa (arRP) and autosomal Leber congenital amaurosis (arLCA). The crumbs (crb) …

PURPOSE: Mutations in the Crumbs homolog 1 (CRB1) gene cause autosomal recessive
retinitis pigmentosa (RP) and Leber congenital amaurosis (LCA). Database searches reveal …

In humans, the Crumbs homologue-1 (CRB1) gene is mutated in progressive types of
autosomal recessive retinitis pigmentosa and Leber congenital amaurosis. The severity of …