DLX3 homeodomain mutations cause tricho-dento-osseous syndrome with novel phenotypes

Pekka Nieminen, Pirjo-Liisa Lukinmaa, Heikki Alapulli, Mirja Methuen, Timo Suojarvi, Sirpa Kivirikko, Jaakko Peltola, Mikko Asikainen, Satu Alaluusua

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalCells, Tissues, Organs
Volume194
Issue number1
Pages (from-to)49-59
Number of pages11
ISSN1422-6405
DOIs
Publication statusPublished - 2011
MoE publication typeA1 Journal article-refereed

Fields of Science

  • Tricho-dento-osseous syndrome
  • DLX3
  • Dentin defect
  • Enamel hypoplasia
  • Taurodontism
  • TDO SYNDROME
  • AMELOGENESIS IMPERFECTA
  • TOOTH DEVELOPMENT
  • DIFFERENTIATION
  • EXPRESSION
  • HETEROGENEITY
  • TAURODONTISM
  • MECHANISMS
  • GENES
  • HAIR
  • 313 Dentistry

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