Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta

Clinical Genetics

Volumn 75, Issue 4, 2009, Pages 401-404

  Hart, P S ^a   Becerik, S ^b   Cogulu, D ^b   Emingil, G ^b   Ozdemir Ozenen, D ^c   Han, S T ^d   Sulima, P P ^d   Firatli, E ^e   Hart, Thomas C ^d  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^b EGE UNIVERSITY   (Turkey)

^c YEDITEPE UNIVERSITY   (Turkey)

^d NATIONAL INSTITUTE OF DENTAL AND CRANIOFACIAL RESEARCH   (United States)

^e ISTANBUL UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN FAM83H; UNCLASSIFIED DRUG;

AMELOGENESIS IMPERFECTA; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL DOMINANT INHERITANCE; DNA DETERMINATION; GENE AMPLIFICATION; GENE EXPRESSION; GENE FUNCTION; GENE LOCUS; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; LETTER; MOSAICISM; MOUTH EXAMINATION; MUTATIONAL ANALYSIS; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; TOOTH DEVELOPMENT; TOOTH RADIOGRAPHY;

AMELOGENESIS IMPERFECTA; CODON, NONSENSE; DNA MUTATIONAL ANALYSIS; FAMILY HEALTH; GENES, DOMINANT; PROTEINS; TURKEY;

EID: 65249125086     PISSN: 00099163     EISSN: 13990004     Source Type: Journal    
DOI: 10.1111/j.1399-0004.2008.01112.x     Document Type: Letter

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