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History
- February 17, 2017.
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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
Author Information
- 1Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, Hyderabad, India;
- 2Graduate Studies, Manipal University, Manipal, India;
- 3Department of Medical Genetics, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India;
- 4Department of Medical Genetics, Kasturba Medical College, Manipal University, Manipal, India.
- ↵#Correspondence to: Dr Ashwin Dalal, Head, Diagnostics Division, Centre for DNA Fingerprinting and Diagnostics, 4-1-714, Tuljaguda Complex Mozamzahi Road, Nampally, Hyderabad Telangana 500001 INDIA, Ph. 040-24749335, Fax: 040 24749448, email: ashwindalal{at}gmail.com, adalal{at}cdfd.org.in
Posted February 17, 2017.
Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis and polydactyly
