TY  - RPRT
TI  - Loss of function mutation of mouse Snap29 on a mixed genetic background phenocopy abnormalities found in CEDNIK and 22q11.2 Deletion Syndrome patients
AU  - Keser, V.
AU  - Boisclair Lachance, J.-F.
AU  - Alam, S. S.
AU  - Lim, Y.
AU  - Scarlata, E.
AU  - Kaur, A.
AU  - Fang, Z. T.
AU  - Lv, S.
AU  - Lachapelle, P.
AU  - O'Flaherty, C.
AU  - Golden, J. A.
AU  - Jerome-Majewska, L. A.
PY  - 2019
DO  - 10.1101/559088
UR  - https://www.biorxiv.org/content/10.1101/559088v1
ID  - 10.1101/559088
ER  -