Issn Print: 1552-4825
Publication Date: 2018/01/01
Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly
Anjana Kar; Shubha R. Phadke; Aneek Das Bhowmik; Ashwin Dalal
Author Information: Diagnostics Division
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