TY  - RPRT
TI  - Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis and polydactyly
AU  - Kar, A.
AU  - Phadke, S. R.
AU  - Bhowmik, A. D.
AU  - Dalal, A.
PY  - 2017
DO  - 10.1101/109124
UR  - https://www.biorxiv.org/content/10.1101/109124v1
ID  - 10.1101/109124
ER  -