Usher syndrome type 1 due to missense mutations on both CDH23 alleles: investigation of mRNA splicing. | Hum Mutat;29(3): 452, 2008 Mar. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Regional Portal

Information and Knowledge for Health

Advanced Search EVID@Easy

Usher syndrome type 1 due to missense mutations on both CDH23 alleles: investigation of mRNA splicing.

Becirovic, Elvir; Ebermann, Inga; Nagy, Ditta; Zrenner, Eberhart; Seeliger, Mathias Wolfgang; Bolz, Hanno Jörn.

Affiliation

Becirovic E; Institute of Human Genetics, University of Cologne, Cologne, Germany.

Hum Mutat ; 29(3): 452, 2008 Mar.

Article in En | MEDLINE | ID: mdl-18273900

Subject(s)

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cadherins / Mutation, Missense / Usher Syndromes Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2008 Document type: Article Affiliation country: Country of publication:

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cadherins / Mutation, Missense / Usher Syndromes Limits: Humans Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2008 Document type: Article Affiliation country: Country of publication: