Published in
Elsevier, Experimental Cell Research, 1(383), p. 111469, 2019
DOI: 10.1016/j.yexcr.2019.06.014
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Single cell analysis of autism patient with bi-allelic NRXN1-alpha deletion reveals skewed fate choice in neural progenitors and impaired neuronal functionality
Journal article published in 2019 by
Matti Lam,
Mohsen Moslem,
Julien Bryois,
Robin J. Pronk 
,
Elias Uhlin,
Ivar Dehnisch Ellström,
Loora Laan,
Jessica Olive,
Rebecca Morse,
Harriet Rönnholm,
Lauri Louhivuori ,
Sergiy V. Korol,
Niklas Dahl,
Per Uhlén,
Britt-Marie Anderlid
and other authors.
,
Elias Uhlin,
Ivar Dehnisch Ellström,
Loora Laan,
Jessica Olive,
Rebecca Morse,
Harriet Rönnholm,
Lauri Louhivuori ,
Sergiy V. Korol,
Niklas Dahl,
Per Uhlén,
Britt-Marie Anderlid
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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