Title : Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6.

Pub. Date : 2007 Jun

PMID : 17503335






1 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 STRA6 encodes an integral cell-membrane protein that favors RA uptake from soluble retinol-binding protein; its transcription is directly regulated by RA levels. Tretinoin signaling receptor and transporter of retinol STRA6 Homo sapiens