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A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod–cone dystrophy phenotype on the Arabian Peninsula

Authors

  1. Correspondence to Dr Arif O Khan, Division of Pediatric Ophthalmology, King Khaled Eye Specialist Hospital, Riyadh 11462, Saudi Arabia; arif.khan{at}mssm.edu
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Citation

Khan AO, Bergmann C, Eisenberger T, et al
A TULP1 founder mutation, p.Gln301*, underlies a recognisable congenital rod–cone dystrophy phenotype on the Arabian Peninsula

Publication history

  • Received July 15, 2014
  • Accepted September 25, 2014
  • First published October 23, 2014.
Online issue publication 
March 23, 2015

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