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Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndrome

Document Type

Article

Author

Petek, E.; Windpassinger, C.; Kroisel, P.M.; Wagner, K.; Vincent, J.B.; Cheung, J.; Boright, A.P.; Scherer, S.W.

Source

In: American Journal of Human Genetics. (American Journal of Human Genetics, 2001, 68(4):848-858)

Subject

Language

English

ISSN

00029297

Online Access

Full Text (ScienceDirect 종량제) Full Text (ScienceDirect O/A) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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