Article

Novel FOXP2 Variant Associated with Speech and Language Dysfunction in a Chinese Family and literature review

2024-01-30

Abstract excerpt

<h4>Background: </h4> Since its initial identification, the Forkhead Box P2 gene ( FOXP2 ) has maintained its singular status as the archetypal monogenic determinant implicated in Mendelian forms of human speech and language impairments. Despite the passage of two decades subsequent to its discovery, extant literature remains disproportionately sparse with regard to case-specific instances and loci of mutational p...

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Literature Corpus work: c5b512af-5aea-56ba-8ae1-74e25efa0109
DOI: 10.21203/rs.3.rs-3892712/v1

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