WNT10A missense mutation associated with a complete Odonto-Onycho-Dermal Dysplasia syndrome

European Journal of Human Genetics

Volumn 17, Issue 12, 2009, Pages 1600-1605

  Nawaz, Sadia ^a   Klar, Joakim ^b   Wajid, Muhammad ^a   Aslam, Muhammad ^a   Tariq, Muhammad ^a   Schuster, Jens ^b   Baig, Shahid Mahmood ^a   Dahl, Niklas ^b  

^a NATIONAL INSTITUTE FOR BIOTECHNOLOGY AND GENETIC ENGINEERING NIBGE   (Pakistan)

^b UPPSALA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

WNT PROTEIN; WNT10A PROTEIN;

ALPHA HELIX; AMINO ACID SEQUENCE; ARTICLE; CHILD; CLINICAL ARTICLE; ECTODERMAL DYSPLASIA; EPIDERMIS; EXON; FEMALE; GENE EXPRESSION; GENE FUNCTION; GENE LOCATION; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENOTYPE; HOMOZYGOSITY; HUMAN; MALE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; ODONTO ONYCHO DERMAL DYSPLASIA; PHENOTYPE; PRIORITY JOURNAL; PROTEIN SECONDARY STRUCTURE; PROTEIN STRUCTURE; SIBLING; SINGLE NUCLEOTIDE POLYMORPHISM; SKIN;

ABNORMALITIES, MULTIPLE; AMINO ACID SEQUENCE; BASE SEQUENCE; ECTODERMAL DYSPLASIA; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION, MISSENSE; PEDIGREE; PROTEIN STRUCTURE, SECONDARY; SYNDROME; WNT PROTEINS;

SOLEIDAE;

EID: 70450233732     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2009.81     Document Type: Article

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