Gene: [05q1/ERVR] Wagner syndrome; erosive vitreoretinopathy; [WGN1 ]
|
CAG |
Brown-1995 demonstrated that erosive vitreoretinopathy and Wagner disease are allelic disorders and genetically distinct from COL2A1-associated Stickler syndrome (GEM:12q131/COL2A1). Authors mapped the disease phenotype to Chr 5q13-14." |
|
REF |
LIN,LOC "Brown DM &: Arch Ophthal, 113, N5, 671-675, 1995 |
|
CLA |
unknown, basic |
|
LOC |
05 q13-14 |
|
MIM |
MIM: 143200 |
|
SYN |
WGN1 |
