Inherited lrp2 dysfunction in human disease and animal models

HIGHLIGHTS

• who: Donnai-Barrow syndrome et al. from the Centre de Recherche des Cordeliers, Paris-Diderot University, France have published the Article: Inherited LRP2 dysfunction in human disease and animal models, in the Journal: Nutritional and signaling defects associated with Lrp2 dysfunction in the neuroectoderm and neuralcrest derived structures of June/29,/2017
• what: Published work clearly shows that LRP2 has site- and time-specific functions.
• future: Studies are necessary to clearly establish the cellular and molecular interdependence of these receptors and clarify their potential as preventive or even therapeutic targets. Future work is . . .
  

   

  

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