Mutation in WNT10A is associated with an autosomal recessive ectodermal dysplasia: The odonto-onycho-dermal dysplasia

American Journal of Human Genetics

Volumn 81, Issue 4, 2007, Pages 821-828

  Adaimy, Lynn ^a   Chouery, Eliane ^a   Mégarbané, Hala ^b   Mroueh, Salman ^b   Delague, Valérie ^c   Nicolas, Elsa ^a   Belguith, Hanen ^a   De Mazancourt, Philippe ^d   Mégarbané, André ^a,e  

^a Université Saint Joseph   (France)

^b AMERICAN UNIVERSITY OF BEIRUT   (Lebanon)

^c INSERM   (France)

^d RAYMOND POINCARÉ HOSPITAL   (France)

^e SAINT JOSEPH UNIVERSITY   (Lebanon)

Author keywords

[No Author keywords available]

Indexed keywords

WNT PROTEIN;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHROMOSOME 2Q; CLINICAL ARTICLE; CONSANGUINITY; CONTROLLED STUDY; ECTODERMAL DYSPLASIA; EXON; FEMALE; GENE; GENE LOCATION; GENE MAPPING; GENETIC SCREENING; HOMOZYGOSITY; HUMAN; MALE; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; ODONTOONYCHODERMAL DYSPLASIA; PRIORITY JOURNAL; WNT10A GENE;

SOLEIDAE;

EID: 35348987509     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/520064     Document Type: Article

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