Human-specific transcriptional regulation of CNS development genes by FOXP2-Reference-Cited by-同舟云学术

Human-specific transcriptional regulation of CNS development genes by FOXP2

Published:2009-11 Issue:7270 Volume:462 Page:213-217
ISSN:0028-0836
Container-title:Nature
language:en
Short-container-title:Nature

Author:

Konopka Genevieve,Bomar Jamee M.,Winden Kellen,Coppola Giovanni,Jonsson Zophonias O.,Gao Fuying,Peng Sophia,Preuss Todd M.,Wohlschlegel James A.,Geschwind Daniel H.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/nature08549.pdf

Reference31 articles.

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2. Lai, C. S., Fisher, S. E., Hurst, J. A., Vargha-Khadem, F. & Monaco, A. P. A forkhead-domain gene is mutated in a severe speech and language disorder. Nature 413, 519–523 (2001)

3. MacDermot, K. D. et al. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. Am. J. Hum. Genet. 76, 1074–1080 (2005)

4. Enard, W. et al. Molecular evolution of FOXP2, a gene involved in speech and language. Nature 418, 869–872 (2002)

5. Zhang, J., Webb, D. M. & Podlaha, O. Accelerated protein evolution and origins of human-specific features: Foxp2 as an example. Genetics 162, 1825–1835 (2002)

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