Gene: [21q223/KNO] Knobloch syndrome (retinal detachment and occipital encephalocele); [KS ]
REF |
PAT,LOC,LIN "Sertie AL &: Hum Mol Genet, 5, 843-847, 1996 |
KEY |
neu, eye |
CLA |
unknown, basic |
LOC |
21 q22.3 |
MIM |
MIM: 267750 |
SYN |
KS |