Perrault syndrome: Evidence for genetic heterogeneity and whole-exome sequencing to identify novel molecular mechanisms


PERÇİN F. E., Li Y., ÇAVDARLI B., Wollnik B.

European Human Genetics Conference 2012, Nürnberg, Germany, 23 June 2012, vol.20, pp.329, (Summary Text)

  • Publication Type: Conference Paper / Summary Text
  • Volume: 20
  • City: Nürnberg
  • Country: Germany
  • Page Numbers: pp.329
  • Ankara Yıldırım Beyazıt University Affiliated: Yes