A claudin subtype that is found localized to TIGHT JUNCTIONS in VASCULAR ENDOTHELIAL CELLS. The protein was initially identified as one of several proteins which are deleted in VELOCARDIOFACIAL SYNDROME and may play an important role in maintaining the integrity of the BLOOD-BRAIN BARRIER.
See also reference (FX) in Slovak
DiGeorgeov syndróm
See also reference (FX) in English
DiGeorge Syndrome
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(1) - MeSH descriptor
subject heading
Number of the records: 1
openseadragon
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