DLX3 c.561_562delCT mutation causes attenuated phenotype of tricho-dento-osseous syndrome

American Journal of Medical Genetics, Part A

Volumn 146, Issue 3, 2008, Pages 343-349

  Wright, J Timothy ^a,d   Hong, Sung P ^a   Simmons, Darrin ^a   Daly, Bill ^a   Uebelhart, Daniel ^b   Luder, Hans U ^c  

^a University of North   (United States)

^b UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^c UNIVERSITY OF ZURICH   (Switzerland)

^d UNIVERSITY OF NORTH CAROLINA   (United States)

Author keywords

Bone; Density; Distal less; DLX3; Enamel; Hair; Hypoplasia

Indexed keywords

PROTEIN DERIVATIVE; PROTEIN DISTALLESS 3; UNCLASSIFIED DRUG;

ARTICLE; BONE DISEASE; GENE MUTATION; HAIR DISEASE; HOMEOBOX; HUMAN; HYPOPLASIA; PHENOTYPE; PRIORITY JOURNAL; SYNDROME; TOOTH DISEASE; TOOTH RADIOGRAPHY; TRICHODONTOOSSEOUS SYNDROME;

AMELOGENESIS IMPERFECTA; BASE SEQUENCE; BONE AND BONES; ECTODERMAL DYSPLASIA; FEMALE; GENES, DOMINANT; HAIR; HOMEODOMAIN PROTEINS; HUMANS; MALE; PEDIGREE; PHENOTYPE; PROTEIN STRUCTURE, TERTIARY; SEQUENCE DELETION; SYNDROME; TRANSCRIPTION FACTORS;

EID: 38949206677     PISSN: 15524825     EISSN: 15524833     Source Type: Journal    
DOI: 10.1002/ajmg.a.32132     Document Type: Article

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