TY  - GEN
TI  - New Pachygyria Syndrome Linked to Actin Regulation Identified: When mutated, CTNNA2 leads to a new form of pachygyria that has a diffuse anterior-posterior gradient with cerebellar hypoplasia, thinning corpus callosum, and absent anterior commissure
SN  - 1552-4833
PY  - 2019///0925
KW  - Actins
KW  - metabolism
KW  - Anterior Commissure, Brain
KW  - abnormalities
KW  - Cerebellum
KW  - Corpus Callosum
KW  - diagnostic imaging
KW  - Developmental Disabilities
KW  - complications
KW  - Humans
KW  - Lissencephaly
KW  - Mutation
KW  - genetics
KW  - Nervous System Malformations
KW  - Syndrome
KW  - alpha Catenin
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/ajmg.a.60672
ER  -