mortality/aging
• reduced postnatal survival similar to Atrx hemizygotes that are heterozygous for Foxg1tm1(cre)Skm
|
growth/size/body
• mutants are smaller at birth
|
nervous system
• not as severe as in Atrx hemizygotes that are heterozygous for Foxg1tm1(cre)Skm
|
• the frontal cortex is reduced in size especially in the caudal-medial cortex similar to Atrx hemizygotes that are heterozygous for Foxg1tm1(cre)Skm but the severity of loss is decreased
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
alpha thalassemia-X-linked intellectual disability syndrome | DOID:0110030 |
OMIM:301040 |
J:95953 |