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Journal Article

Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

Julie Gauthier; Tabrez J. Siddiqui; Peng Huashan; Daisaku Yokomaku; Fadi F. Hamdan; Nathalie Champagne; Mathieu Lapointe; Dan Spiegelman; Anne Noreau; Ronald G. Lafrenière; Ferid Fathalli; Ridha Joober; Marie-Odile Krebs; Lynn E. DeLisi; Laurent Mottron; Éric Fombonne; Jacques L. Michaud; Pierre Drapeau; Salvatore Carbonetto; Ann Marie Craig; Guy A. Rouleau
Human Genetics · Vol. 130, Issue 4 · pp. 563-573 · 2011
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Abstract

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Bibliographic Information

JournalHuman Genetics
PublisherSpringer
Publication Date2011-10-01
Publication Year2011
Volume130
Issue4
Pages563-573
Document TypeJournal Article
Print ISSN0340-6717
eISSN1432-1203
DOI10.1007/s00439-011-0975-z

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NARA Access Coverage1964-01-01~Current
Journal Homepagehttps://www.springer.com/journal/439
Publisher PageOpen Publisher Page
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