Keratoderma-Deafness-Mucocutaneous Syndrome Associated with Phe142Leu in the GJB2 Gene. uri icon

Overview

publication date

  • November 1, 2019

Research

keywords

  • Connexins
  • Hearing Loss, Sensorineural
  • Keratoderma, Palmoplantar
  • Mutation
  • Polymorphism, Single Nucleotide
  • Skin

Identity

Scopus Document Identifier

  • 85074343345

Digital Object Identifier (DOI)

  • 10.2340/00015555-3291

PubMed ID

  • 31408183

Additional Document Info

volume

  • 99

issue

  • 12