Mutations in PMCA2 and hereditary deafness: A molecular analysis of the pump defect

Cell Calcium

Volumn 50, Issue 6, 2011, Pages 569-576

  Giacomello, Marta ^a,b   de Mario, Agnese ^a   Lopreiato, Raffaele ^b   Primerano, Simona ^a   Campeol, Mara ^a   Brini, Marisa ^b   Carafoli, Ernesto ^a  

^a VENETIAN INSTITUTE OF MOLECULAR MEDICINE   (Italy)

^b UNIVERSITY OF PADOVA   (Italy)

Author keywords

Calcium signaling; Deafness

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); CADHERIN 23; CALCIUM ION; PROTEIN PMCA2; UNCLASSIFIED DRUG;

ARTICLE; CALCIUM SIGNALING; CALCIUM TRANSPORT; CONTROLLED STUDY; GENE MUTATION; HEARING IMPAIRMENT; HEREDITARY DEAFNESS; HUMAN; HUMAN CELL; MOLECULAR GENETICS; MUTANT; PRIORITY JOURNAL;

MURINAE; MUS;

EID: 82855175101     PISSN: 01434160     EISSN: 15321991     Source Type: Journal    
DOI: 10.1016/j.ceca.2011.09.004     Document Type: Article

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