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Original Article
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly
- Correspondence to Dr Sajid Malik, Human Genetics Program, Department of Animal Sciences, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan; malik{at}qau.edu.pk and Professor Aslıhan Tolun, Department of Molecular Biology and Genetics, Boğaziçi University, Istanbul, Turkey-34342; tolun{at}boun.edu.tr
Citation
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly
Publication history
- Received April 27, 2017
- Revised October 16, 2017
- Accepted October 29, 2017
- First published November 10, 2017.
Online issue publication
February 22, 2018
Article Versions
- Previous version (10 November 2017).
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