Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome

Autor:	Yan Bai, Jiaxin Xu, Aiwen Yi, Jing Xin, Mingwei Huang
Rok vydání:	2021
Předmět:	Genetics Genotype FOXG1 syndrome Forkhead Transcription Factors Nerve Tissue Proteins General Medicine Biology medicine.disease Genotype phenotype FOXG1 Epilepsy Phenotype Neurology Clinical heterogeneity medicine Humans Neurology (clinical)
Zdroj:	Seizure. 89:45-47
ISSN:	1059-1311
DOI:	10.1016/j.seizure.2021.04.023
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae7480efcfe9c62bb800ff98b3ae5267 https://doi.org/10.1016/j.seizure.2021.04.023 Zobrazit plný text záznamu Full Text from ScienceDirect