Modification of human hearing loss by plasma-membrane calcium pump PMCA2

New England Journal of Medicine

Volumn 352, Issue 15, 2005, Pages 1557-1564

  Schultz, Julie M ^a   Yang, Yandan ^a   Caride, Ariel J ^c   Filoteo, Adelaida G ^c   Penheiter, Alan R ^d   Lagziel, Ayala ^a   Morell, Robert J ^a   Mohiddin, Saidi A ^b   Fananapazir, Lameh ^b   Madeo, Anne C ^a   Penniston, John T ^e   Griffith, Andrew J ^a  

^a NATIONAL INSTITUTES OF HEALTH   (United States)

^b NATIONAL HEART LUNG AND BLOOD INSTITUTE   (United States)

^c MAYO GRADUATE SCHOOL   (United States)

^d MAYO CLINIC   (United States)

^e MASSACHUSETTS GENERAL HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); CADHERIN; CADHERIN 23; MYOSIN; MYOSIN VI; PROTEIN PMCA2; UNCLASSIFIED DRUG; ATP2B2 PROTEIN, HUMAN; CATION TRANSPORT PROTEIN; CDH23 PROTEIN, HUMAN; PLASMA MEMBRANE CALCIUM TRANSPORTING ADENOSINE TRIPHOSPHATASE;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; CDH23 GENE; CELL MEMBRANE; CLINICAL ARTICLE; DISEASE SEVERITY; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC VARIABILITY; HEARING LOSS; HOMOZYGOSITY; HUMAN; MALE; MYO6 GENE; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SIBLING; ALLELE; CASE REPORT; CLASSIFICATION; GENETICS; GENOTYPE; HETEROZYGOTE; MIDDLE AGED; MISSENSE MUTATION; MULTIFACTORIAL INHERITANCE; PEDIGREE; PHENOTYPE; POINT MUTATION; RECESSIVE GENE;

ADULT; ALLELES; CADHERINS; CALCIUM-TRANSPORTING ATPASES; CATION TRANSPORT PROTEINS; FEMALE; GENES, RECESSIVE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HETEROZYGOTE; HUMANS; MALE; MIDDLE AGED; MULTIFACTORIAL INHERITANCE; MUTATION, MISSENSE; PEDIGREE; PHENOTYPE; PLASMA MEMBRANE CALCIUM-TRANSPORTING ATPASES; POINT MUTATION; SIBLINGS;

EID: 20144389358     PISSN: 00284793     EISSN: None     Source Type: Journal    
DOI: 10.1056/NEJMoa043899     Document Type: Article

References (24)

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