PhenomeGene — Human Disease Gene Website SeriesTAF2

Publications

Lesieur-Sebellin M et al. Phenotype associated with TAF2 biallelic mutations: A clinical description of four individuals and review of the literature.Eur J Med Genet. 2021;64(11):104323. PMID: 34474177.

Najmabadi H et al. Deep sequencing reveals 50 novel genes for recessive cognitive disorders. Nature. 2011;478(7367):57-63. PMID: 21937992.

Halevy A et al. Microcephaly-thin corpus callosum syndrome maps to 8q23.2-q24.12. Pediatr Neurol. 2012;46(6):363-8. PMID: 22633631.

Grozeva D et al. Targeted Next-Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability. Hum Mutat. 2015;36(12):1197-1204. PMID: 26350204.