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Dive into the research topics of 'Impaired permeabilty to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness'. Together they form a unique fingerprint.- Sort by
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Martina Beltramello, Valeria Piazza, Feliksas F. Bukauskas, Tullio Pozzan, Fabio Mammano
Research output: Contribution to journal › Article › peer-review