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PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier. [electronic resource] by
- Pichery, Mélanie
- Huchenq, Anne
- Sandhoff, Roger
- Severino-Freire, Maella
- Zaafouri, Sarra
- Opálka, Lukáš
- Levade, Thierry
- Soldan, Vanessa
- Bertrand-Michel, Justine
- Lhuillier, Emeline
- Serre, Guy
- Maruani, Annabel
- Mazereeuw-Hautier, Juliette
- Jonca, Nathalie
Producer: 20171010
In:
Human molecular genetics vol. 26
Availability: No items available.
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