Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II.

Human mutation

Volumn 29, Issue 3, 2008, Pages 451-

  Dreyer, B ^a   Brox, Vigdis ^a   Tranebjaerg, Lisbeth ^a   Rosenberg, Thomas ^a   Sadeghi, Andrè M ^a   Möller, Claes ^a   Nilssen, Oivind ^a  

^a UNIVERSITY OF TROMSØ   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

CLRN1 PROTEIN, HUMAN; DNA; MEMBRANE PROTEIN; SCLEROPROTEIN; UNCLASSIFIED DRUG; USH2A PROTEIN, HUMAN;

ARTICLE; CLASSIFICATION; EXON; FEMALE; GENE DELETION; GENETICS; GENOTYPE; HUMAN; INTRON; MALE; MISSENSE MUTATION; MUTATION; NUCLEOTIDE SEQUENCE; SCANDINAVIA; STOP CODON; USHER SYNDROME;

CODON, NONSENSE; DNA; DNA MUTATIONAL ANALYSIS; EXONS; EXTRACELLULAR MATRIX PROTEINS; FEMALE; GENOTYPE; HUMANS; INTRONS; MALE; MEMBRANE PROTEINS; MUTATION; MUTATION, MISSENSE; SCANDINAVIA; SEQUENCE DELETION; USHER SYNDROMES;

EID: 41449108355     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9524     Document Type: Article

References (0)