Work

Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

Year: 2005

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1086/430841

Authors: Kay D. MacDermot, Elena Bonora, Nuala Sykes, Anne-Marie Coupe, Cecilia S.L. Lai, Sonja C. Vernes, Faraneh Vargha-Khadem, Fiona McKenzie, Robert L. Smith, Anthony P. Monaco, Simon E. Fisher

Institutions: Centre for Human Genetics, University of Oxford, Imperial College London, University College London, John Hunter Children's Hospital

Language: English

Topic: Genetics and Neurodevelopmental Disorders

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Wellcome Trust, Royal Society, Clarendon Fund

OpenAlex ID: W1963818866

FWCI: 10.98

Cites: 34

Cited by: 406

Related to: 10