A novel missense mutation in the ectodysplasin-A (EDA) gene underlies X-linked recessive nonsyndromic hypodontia

International Journal of Dermatology

Volumn 49, Issue 12, 2010, Pages 1399-1402

  Ayub, Muhammad ^a,c   Ur Rehman, Fazal ^b   Yasinzai, Masoom ^c   Ahmad, Wasim ^a  

^a Department of Biochemistry ^*  (Pakistan)

^b QUAID I AZAM UNIVERSITY   (Pakistan)

^c UNIVERSITY OF BALOCHISTAN   (Pakistan)

Author keywords

[No Author keywords available]

Indexed keywords

ECTODYSPLASIN A; GLUTAMINE; HISTIDINE; TUMOR NECROSIS FACTOR;

AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHROMOSOME XQ; DNA SEQUENCE; EXON; GENE AMPLIFICATION; GENE MAPPING; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; GENETIC POLYMORPHISM; GENETIC SCREENING; GENOTYPE; HUMAN; HYPODONTIA; MALE; MICROSATELLITE MARKER; MISSENSE MUTATION; MORPHOGENESIS; PAKISTAN; POLYMERASE CHAIN REACTION; RNA SPLICING; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; SIGNAL TRANSDUCTION; X CHROMOSOME LINKED DISORDER; X LINKED RECESSIVE NONSYNDROMIC HYPODONTIA;

CHILD; CHROMOSOMES, HUMAN, X; ECTODERMAL DYSPLASIA 1, ANHIDROTIC; ECTODYSPLASINS; FEMALE; GENOTYPE; HUMANS; MALE; MUTATION, MISSENSE; PEDIGREE; SIGNAL TRANSDUCTION;

EID: 78649416901     PISSN: 00119059     EISSN: 13654632     Source Type: Journal    
DOI: 10.1111/j.1365-4632.2010.04596.x     Document Type: Article

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