Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1

Human Genetics

Volumn 107, Issue 1, 2000, Pages 89-91

  Jacobi, Felix K ^a   Broghammer, Martina ^a   Pesch, Katrin ^a   Zrenner, Eberhart ^a   Berger, Wolfgang ^b   Meindl, Alfons ^c   Pusch, Carsten M ^a  

^a UNIVERSITY HOSPITAL TÜBINGEN   (Germany)

^b MAX PLANCK INSTITUTE FOR MOLECULAR GENETICS   (Germany)

^c UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

G PROTEIN COUPLED RECEPTOR;

ARTICLE; CHROMOSOME XP; CONTROLLED STUDY; DNA SEQUENCE; GENE LOCATION; GENE MAPPING; HUMAN; HUMAN CELL; NIGHT BLINDNESS; PRIORITY JOURNAL; SIGNAL TRANSDUCTION; SOUTHERN BLOTTING;

EID: 0033873202     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390000337     Document Type: Article

References (9)

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