Imaging genetics of FOXP2 in dyslexia

Wilcke, A.; Ligges, C.; Burkhardt, J.; Alexander, M.; Wolf, C.; Quente, E.; Ahnert, P.; Hoffmann, P.; Becker, A.; Müller-Myhsok, B.; Cichon, S.; Boltze, J.; Kirsten, H.

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Imaging genetics of FOXP2 in dyslexia

Wilcke, A., Ligges, C., Burkhardt, J., Alexander, M., Wolf, C., Quente, E., et al. (2012). Imaging genetics of FOXP2 in dyslexia. European Journal of Human Genetics, 20(2), 224-229.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-8CD2-A Version Permalink: https://hdl.handle.net/11858/00-001M-0000-000E-8CD3-8

Genre: Journal Article

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Creators:
Wilcke, A., Author
Ligges, C., Author
Burkhardt, J., Author
Alexander, M., Author
Wolf, C.¹, Author
Quente, E., Author
Ahnert, P., Author
Hoffmann, P., Author
Becker, A.², Author
Müller-Myhsok, B.¹, Author
Cichon, S., Author
Boltze, J., Author
Kirsten, H., Author

Affiliations:
1AG Müller-Myhsok, Bertram, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607154
2AG Müller, Marianne, Florian Holsboer (Direktor), Max Planck Institute of Psychiatry, Max Planck Society, ou_1607153

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Language(s): eng - English

Dates: Date issued: 2012-02

Publication Status: Issued

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Identifiers: eDoc: 582164
ISI: 000299323000024

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Title: European Journal of Human Genetics

Source Genre: Journal

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Pages: - Volume / Issue: 20 (2) Sequence Number: - Start / End Page: 224 - 229 Identifier: ISSN: 1018-4813