LINS, a modulator of the WNT signaling pathway, is involved in human cognition

Orphanet Journal of Rare Diseases

Volumn 8, Issue 1, 2013, Pages

  Akawi, Nadia A ^a   Al Jasmi, Fatma ^a   Al Shamsi, Aisha M ^b   Ali, Bassam R ^a   Al Gazali, Lihadh ^a  

^a UNITED ARAB EMIRATES UNIVERSITY   (United Arab Emirates)

^b TAWAM HOSPITAL   (United Arab Emirates)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; COGNITION; CONTROLLED STUDY; DROSOPHILA; EXOME; EXON; EXON SKIPPING; FEMALE; GENE; GENE MUTATION; GENE SEQUENCE; HOMOZYGOSITY; HUMAN; INTELLECTUAL IMPAIRMENT; INTRON; LINS GENE; MALE; MICROCEPHALY; OLIGONUCLEOTIDE PROBE; RNA ANALYSIS; RNA SPLICING; RNA TRANSLATION; WNT SIGNALING PATHWAY;

CHILD; CHILD, PRESCHOOL; COGNITION; EXONS; FEMALE; GENES, RECESSIVE; HUMANS; INTELLECTUAL DISABILITY; MALE; MUTATION; PEDIGREE; PROTEINS; WNT SIGNALING PATHWAY;

EID: 84879046081     PISSN: None     EISSN: 17501172     Source Type: Journal    
DOI: 10.1186/1750-1172-8-87     Document Type: Article

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