Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability

Metabolic Brain Disease

Volumn 31, Issue 4, 2016, Pages 901-907

  Alkhateeb, Asem M ^a,b   Aburahma, Samah K ^b   Habbab, Wesal ^a   Thompson, I Richard ^a  

^a HAMAD BIN KHALIFA UNIVERSITY   (Qatar)

^b JORDAN UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Jordan)

Author keywords

C10orf2; Exome; Intellectual disability; RARS2; WWOX

Indexed keywords

ARGININE TRANSFER RNA LIGASE; C10ORF10 PROTEIN, HUMAN; PROTEIN; RARS2 PROTEIN, HUMAN; TUMOR SUPPRESSOR PROTEIN; WW DOMAIN CONTAINING OXIDOREDUCTASE; WWOX PROTEIN, HUMAN;

ARAB; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; EXOME; FEMALE; GENETICS; GENOTYPE; HUMAN; INTELLECTUAL IMPAIRMENT; MALE; MUTATION; PEDIGREE; PHENOTYPE;

ARABS; ARGININE-TRNA LIGASE; CONSANGUINITY; DNA MUTATIONAL ANALYSIS; EXOME; FEMALE; GENOTYPE; HUMANS; INTELLECTUAL DISABILITY; MALE; MUTATION; PEDIGREE; PHENOTYPE; PROTEINS; TUMOR SUPPRESSOR PROTEINS; WW DOMAIN-CONTAINING OXIDOREDUCTASE;

EID: 84964467788     PISSN: 08857490     EISSN: 15737365     Source Type: Journal    
DOI: 10.1007/s11011-016-9827-9     Document Type: Article

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