Meckel syndrome type 8 is an autosomal recessive disorder caused by mutations in the TCTN2 gene.
Meckel syndrome | ||||
Meckel syndrome 02 | ||||
Meckel syndrome 03 | ||||
Meckel syndrome 05 | ||||
Meckel syndrome 06 | ||||
Meckel syndrome 08 | ||||
TCTN2 | ||||
Meckel syndrome 09 | ||||
Meckel syndrome 10 | ||||
Meckel syndrome 11 | ||||
Meckel syndrome 13 | ||||
1. |
Shaheen R et al. (2011) A TCTN2 mutation defines a novel Meckel Gruber syndrome locus. |
2. |
OMIM.ORG article Omim 613885 |