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Original Article
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly

Authors

  1. 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
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Citation

Yıldız Bölükbaşı E, Mumtaz S, Afzal M, et al
Homozygous mutation in CEP19, a gene mutated in morbid obesity, in Bardet-Biedl syndrome with predominant postaxial polydactyly

Publication history

  • Received 27 April 2017
  • Revised 16 October 2017
  • Accepted 29 October 2017
  • Published online 10 November 2017.

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