reference/25146990

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25146990

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bibliographicCitation	Ching MS, Shen Y, Tan WH, Jeste SS, Morrow EM, Chen X, Mukaddes NM, Yoo SY, Hanson E, Hundley R, Austin C, Becker RE, Berry GT, Driscoll K, Engle EC, Friedman S, Gusella JF, Hisama FM, Irons MB, Lafiosca T, LeClair E, Miller DT, Neessen M, Picker JD, Rappaport L, Rooney CM, Sarco DP, Stoler JM, Walsh CA, Wolff RR, Zhang T, Nasir RH, Wu BL; Children's Hospital Boston Genotype Phenotype Study Group. Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders. Am J Med Genet B Neuropsychiatr Genet. 2010 Jun 05;153B(4):937–47. PMID: 20468056; PMCID: PMC3001124.
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date	2010-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC3001124 https://doi.org/10.1002/ajmg.b.31063 https://pubmed.ncbi.nlm.nih.gov/20468056
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Deletions of NRXN1 (neurexin‐1) predispose to a wide spectrum of developmental disorders
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