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Journal of Clinical Investigation, ISSN 0021-9738, 11/2012, Volume 122, Issue 11, pp. 3990 - 4002
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, pp. e78496 - e78496
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2014, Volume 46, Issue 12, pp. 1283 - 1292
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 04/2012, Volume 90, Issue 4, pp. 685 - 688
Journal Article
Journal Article
Acta Dermato-Venereologica, ISSN 0001-5555, 05/2018, Volume 98, Issue 5, pp. 534 - 535
Journal Article
The EMBO Journal, ISSN 0261-4189, 08/2018, Volume 37, Issue 15, p. n/a
Journal Article
Human Mutation, ISSN 1059-7794, 09/2016, Volume 37, Issue 9, pp. 847 - 864
Journal Article
BMC Medical Genetics, ISSN 1471-2350, 08/2011, Volume 12, Issue 1, pp. 106 - 106
Background: Heterozygous copy-number and missense variants in CNTNAP2 and NRXN1 have repeatedly been associated with a wide spectrum of neuropsychiatric... 
AUTISM | DISRUPTION | GENE | LA-TOURETTE-SYNDROME | STRUCTURAL VARIANTS | GENETICS & HEREDITY | SCHIZOPHRENIA | DISORDERS | NEUREXIN SUPERFAMILY | DELETIONS | GENOME | Cellular proteins | Genetic aspects | Research | Health aspects | Mental illness | Risk factors | Index Medicus
Journal Article
Human Mutation, ISSN 1059-7794, 04/2017, Volume 38, Issue 4, pp. 451 - 459
Journal Article