Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

Leber congenital amaurosis 17

Leber congenital amaurosis 17 is an autosomal recessive disorder caused by mutations of the GDF6 gene.

Systematic

Leber congenital amaurosis
Leber congenital amaurosis 01
Leber congenital amaurosis 02
Leber congenital amaurosis 03
Leber congenital amaurosis 04
Leber congenital amaurosis 05
Leber congenital amaurosis 06
Leber congenital amaurosis 07
Leber congenital amaurosis 08
Leber congenital amaurosis 09
Leber congenital amaurosis 10
Leber congenital amaurosis 11
Leber congenital amaurosis 12
Leber congenital amaurosis 13
Leber congenital amaurosis 14
Leber congenital amaurosis 15
Leber congenital amaurosis 16
Leber congenital amaurosis 17
GDF6
Leber congenital amaurosis 18

References:

1.

Asai-Coakwell M et. al. (2013) Contribution of growth differentiation factor 6-dependent cell survival to early-onset retinal dystrophies.

[^]
Update: Sept. 26, 2018