Molecular analysis of NPAS3 functional domains and variants
Author:
Funder
Canadian Institutes of Health Research
Publisher
Springer Science and Business Media LLC
Subject
Molecular Biology
Link
http://link.springer.com/content/pdf/10.1186/s12867-018-0117-4.pdf
Reference80 articles.
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3. Pickard BS, Malloy MP, Porteous DJ, Blackwood DH, Muir WJ. Disruption of a brain transcription factor, NPAS3, is associated with schizophrenia and learning disability. Am J Med Genet B Neuropsychiatr Genet. 2005;136B(1):26–32.
4. Kamnasaran D, Chen CP, Devriendt K, Mehta L, Cox DW. Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes. Genomics. 2005;85(5):608–21.
5. Rosenfeld JA, Ballif BC, Martin DM, Aylsworth AS, Bejjani BA, Torchia BS, Shaffer LG. Clinical characterization of individuals with deletions of genes in holoprosencephaly pathways by aCGH refines the phenotypic spectrum of HPE. Hum Genet. 2010;127(4):421–40.
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