Recurrent heterozygous missense mutation, p.Gly573Ser, in the TRPV3 gene in an Indian boy with sporadic Olmsted syndrome

  • J. E. Lai-Cheong
  • , G. Sethuraman
  • , M. Ramam
  • , K. Stone
  • , M. A. Simpson
  • , J. A. McGrath

Research output: Contribution to journal › Article › peer-review

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Biochemistry, Genetics and Molecular Biology