Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.

Human mutation

Volumn 17, Issue 6, 2001, Pages 520-

  Martinez Gimeno, M ^a   Maseras, M ^a   Baiget, M ^a   Beneito, M ^a   Antinolo G ^a   Ayuso, C ^a   Carballo, M ^a  

^a Servei de Laboratori   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

BASIC LEUCINE ZIPPER TRANSCRIPTION FACTOR; DNA; DNA BINDING PROTEIN; EYE PROTEIN; NRL PROTEIN, HUMAN;

ARTICLE; CHEMISTRY; DOMINANT GENE; FAMILY HEALTH; FEMALE; GENETICS; HUMAN; MALE; MISSENSE MUTATION; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; RETINITIS PIGMENTOSA; SINGLE STRAND CONFORMATION POLYMORPHISM;

BASE SEQUENCE; BASIC-LEUCINE ZIPPER TRANSCRIPTION FACTORS; DNA; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; EYE PROTEINS; FAMILY HEALTH; FEMALE; GENES, DOMINANT; HUMANS; MALE; MUTATION; MUTATION, MISSENSE; PEDIGREE; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RETINITIS PIGMENTOSA;

MLCS; MLOWN;

EID: 0035377437     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.1135     Document Type: Article

References (0)