Associated Papers
Overview and expansion of CEP85L-associated lissencephaly.
Schumann I et al.
European Journal of Medical Genetics, 2025
Diagnostic utility of exome sequencing followed by research reanalysis in human brain malformations.
Kooshavar D et al.
Brain Communications, 2024
Further characterization of CEP85L-associated lissencephaly type 10: Report of a three-generation family and review of the literature.
Leduc-Pessah H et al.
American Journal of Medical Genetics. Part A, 2023
Posterior Lissencephaly Associated with Subcortical Band Heterotopia Due to a Variation in the CEP85L Gene: A Case Report and Refining of the Phenotypic Spectrum.
Contrò G et al.
Genes, 2021
Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly.
Tsai MH et al.
Neuron, 2020
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