학술논문
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)
Document Type
Author
Source
In Stem Cell Research May 2021 53
Subject
Language
ISSN
1873-5061