Concepedia

Publication | Open Access

De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment

DOIFull Paper Access

233

Citations

30

References

2010

Year

Fadi F. Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie‐Odile Krebs, Ridha Joober,
The American Journal of Human Genetics

References

YearCitations

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