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

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

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

Affiliation

Schultz JM; Section on Human Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Md 20850, USA.

N Engl J Med ; 352(15): 1557-64, 2005 Apr 14.

Article in En | MEDLINE | ID: mdl-15829536

Subject(s)

Cadherins/genetics; Calcium-Transporting ATPases/genetics; Hearing Loss, Sensorineural/genetics; Multifactorial Inheritance; Mutation, Missense; Adult; Alleles; Cadherin Related Proteins; Cation Transport Proteins; Female; Genes, Recessive; Genotype; Hearing Loss, Sensorineural/classification; Heterozygote; Humans; Male; Middle Aged; Pedigree; Phenotype; Plasma Membrane Calcium-Transporting ATPases; Point Mutation; Siblings

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Cadherins / Calcium-Transporting ATPases / Mutation, Missense / Multifactorial Inheritance / Hearing Loss, Sensorineural Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: N Engl J Med Year: 2005 Document type: Article Affiliation country: United States

Search on Google

Add to My VHL

XML

PubMed Links