TY  - RPRT
TI  - A Point Mutation in the RNA Recognition Motif of CSTF2 Associated with Intellectual Disability in Humans Causes Defects in 3' End Processing
AU  - Grozdanov, P. N.
AU  - Masoumzadeh, E.
AU  - Kalscheuer, V. M.
AU  - Bienvenu, T.
AU  - Billuart, P.
AU  - Latham, M. P.
AU  - Delrue, M.-A.
AU  - MacDonald, C. C.
PY  - 2020
DO  - 10.1101/2020.01.02.893107
UR  - https://www.biorxiv.org/content/10.1101/2020.01.02.893107v1
ID  - 10.1101/2020.01.02.893107
ER  -