TY  - GEN
AU  - Tsai,Meng-Han
AU  - Muir,Alison M
AU  - Wang,Won-Jing
AU  - Kang,Yi-Ning
AU  - Yang,Kun-Chuan
AU  - Chao,Nian-Hsin
AU  - Wu,Mei-Feng
AU  - Chang,Ying-Chao
AU  - Porter,Brenda E
AU  - Jansen,Laura A
AU  - Sebire,Guillaume
AU  - Deconinck,Nicolas
AU  - Fan,Wen-Lang
AU  - Su,Shih-Chi
AU  - Chung,Wen-Hung
AU  - Almanza Fuerte,Edith P
AU  - Mehaffey,Michele G
AU  - Ng,Ching-Ching
AU  - Chan,Chung-Kin
AU  - Lim,Kheng-Seang
AU  - Leventer,Richard J
AU  - Lockhart,Paul J
AU  - Riney,Kate
AU  - Damiano,John A
AU  - Hildebrand,Michael S
AU  - Mirzaa,Ghayda M
AU  - Dobyns,William B
AU  - Berkovic,Samuel F
AU  - Scheffer,Ingrid E
AU  - Tsai,Jin-Wu
AU  - Mefford,Heather C
TI  - Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly
SN  - 1097-4199
PY  - 2020///0811
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Animals
KW  - Centrosome
KW  - pathology
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Aberrations
KW  - Classical Lissencephalies and Subcortical Band Heterotopias
KW  - diagnostic imaging
KW  - Cytoskeletal Proteins
KW  - genetics
KW  - Female
KW  - Gene Knockdown Techniques
KW  - Genetic Variation
KW  - Heterozygote
KW  - Humans
KW  - Infant
KW  - Magnetic Resonance Imaging
KW  - Male
KW  - Mice
KW  - Mutation
KW  - Oncogene Proteins, Fusion
KW  - Pedigree
KW  - Seizures
KW  - etiology
KW  - Young Adult
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.neuron.2020.01.027
ER  -