Concepedia

Publication | Open Access

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

DOIFull Paper Access

275

Citations

34

References

2011

Year

Julie Gauthier, Tabrez J. Siddiqui, Huashan Peng, Daisaku Yokomaku, Fadi F. Hamdan, Nathalie Champagne, Mathieu Lapointe, Dan Spiegelman, Anne Noreau, Ronald G. Lafrenière,
Human Genetics

References

YearCitations

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