R32W variant in Connexin 31: Mutation or polymorphism for deafness and skin disease? (multiple letters) [2]

N. LoÓpez-Bigas, R. Rabionet, M. L. Arboneés, X. Estivill, David Kelsell

Research output: Contribution to journalLetter

9 Citations (Scopus)
Original languageEnglish
Number of pages1
JournalEuropean Journal of Human Genetics
Issue number1
Publication statusPublished - 1 Jan 2001

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

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