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Paper Details

Derivation of four iPSC lines from a male ASD patient carrying a deletion in the middle coding region of NRXN1α gene (NUIGi039-A and NUIGi039-B) and a male sibling control (NUIGi040-A and NUIGi040-B).
Stem Cell Res
0
2021
ASD, NRXN1, NRXN1 gene, NUIGi039-A, NUIGi039-B, NUIGi040, autism spectrum disorder, deletion regions, iPSC lines, iPSCs, induced pluripotent stem cells, neurodevelopmental/neuropsychiatric disorders, patient, splicing variants
Author NameAffiliation
Xiaohong QianBeijing Proteome Research Center, National Center for Protein Sciences, Beijing Institute of Proteomics
Sally Ann LynchMater Misericordiae University Hospital, University College Dublin
Louise GallagherTrinity Institute of Neuroscience, Trinity College Dublin
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Release 1.2