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Browsing by Author Bodemer, C.

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Clinical expression and new SPINK5 splicing defects in Netherton syndrome: unmasking a frequent founder synonymous mutation and unconventional intronic mutationsLacroix, M.; Lacaze-Buzy, L.; Furio, L.; Tron, E.; Valari, M.; Van der Wier, G.; Bodemer, C.; Bygum, A.; Bursztejn, A. C.; Gaitanis, G.; Paradisi, M.; Stratigos, A.; Weibel, L.; Deraison, C.; Hovnanian, A.24-Nov-2015-
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