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

Cells Tissues Organs

Volumn 194, Issue 1, 2011, Pages 49-59

  Nieminen, Pekka ^a   Lukinmaa, Pirjo Liisa ^a   Alapulli, Heikki ^b   Methuen, Mirja ^c   Suojärvi, Timo ^b   Kivirikko, Sirpa ^b   Peltola, Jaakko ^b   Asikainen, Mikko ^a   Alaluusua, Satu ^a,b  

^a UNIVERSITY OF HELSINKI   (Finland)

^b HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^c KUOPIO UNIVERSITY HOSPITAL   (Finland)

Author keywords

Dentin defect; DLX3; Enamel hypoplasia; Taurodontism; Tricho dento osseous syndrome

Indexed keywords

HOMEODOMAIN PROTEIN; PROTEIN DLX3; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CRANIOFACIAL MORPHOLOGY; DENTIN; DISEASE SEVERITY; ECTODERMAL DYSPLASIA; ENAMEL; GENE MUTATION; GENETIC ANALYSIS; HAPLOINSUFFICIENCY; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; LOSS OF FUNCTION MUTATION; MISSENSE MUTATION; MOLAR TOOTH; MUTATIONAL ANALYSIS; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; TOOTH ABSCESS; TOOTH MALFORMATION; TOOTH PULP; TRICHO DENTO OSSEOUS SYNDROME;

AMINO ACID SEQUENCE; BASE SEQUENCE; DENTAL ENAMEL HYPOPLASIA; DNA MUTATIONAL ANALYSIS; FAMILY; FINLAND; GENES, HOMEOBOX; HAIR DISEASES; HAPLOINSUFFICIENCY; HOMEODOMAIN PROTEINS; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; PHENOTYPE; TRANSCRIPTION FACTORS;

EID: 79959377743     PISSN: 14226405     EISSN: 14226421     Source Type: Journal    
DOI: 10.1159/000322561     Document Type: Article

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