EYA4, Deleted in a case with middle interhemispheric variant of holoprosencephaly, interacts with SIX3 both physically and functionally

Human Mutation

Volumn 30, Issue 10, 2009, Pages 946-955

  Abe, Yuichi ^a,b,c   Oka, Akira ^b   Mizuguchi, Masashi ^b   Igarashi, Takashi ^b   Ishikawa, Shumpei ^d   Aburatani, Hiroyuki ^d   Yokoyama, Shigetoshi ^c   Asahara, Hiroshi ^c   Nagao, Kazuaki ^a   Yamada, Masao ^c   Miyashita, Toshiyuki ^a  

^a KITASATO UNIVERSITY   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c NATIONAL RESEARCH INSTITUTE FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

^d UNIVERSITY OF TOKYO   (Japan)

Author keywords

Eya4; Holoprosencephaly; Middle interhemispheric variant; SIX3

Indexed keywords

EYA4 PROTEIN, HUMAN; EYE PROTEIN; HOMEODOMAIN PROTEIN; NERVE PROTEIN; PRIMER DNA; SINE OCULIS HOMEOBOX HOMOLOG 3 PROTEIN; TRANSACTIVATOR PROTEIN;

ANIMAL; ARTICLE; CASE REPORT; CELL LINE; DNA MICROARRAY; GENE DELETION; GENETICS; HOLOPROSENCEPHALY; HUMAN; IN SITU HYBRIDIZATION; INFANT; MALE; METABOLISM; MOUSE; NUCLEOTIDE SEQUENCE; PROTEIN BINDING;

ANIMALS; BASE SEQUENCE; CELL LINE; DNA PRIMERS; EYE PROTEINS; GENE DELETION; HOLOPROSENCEPHALY; HOMEODOMAIN PROTEINS; HUMANS; IN SITU HYBRIDIZATION; INFANT; MALE; MICE; NERVE TISSUE PROTEINS; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PROTEIN BINDING; TRANS-ACTIVATORS;

EID: 73349110981     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21094     Document Type: Article

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