The murine tub (rd5) mutation is not associated with a primary axonemal defect

Cell and Tissue Research

Volumn 291, Issue 3, 1998, Pages 489-495

  Ohlemiller, Kevin K ^a   Ogilvie, Judith Mosinger ^a,b   Lett, Jaclynn M ^a   Hughes, Ruth M ^a   LaRegina, Marie C ^b   Olson, Lisa M ^b  

^a CENTRAL INSTITUTE FOR THE DEAF   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Alstrom's syndrome; Barder Biedl syndrome; Cilia; Cochlea; Mouse C57BL 6J; Photoreceptors; Retina; Sperm; Usher's syndrome

Indexed keywords

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; AXONEME; CELL ULTRASTRUCTURE; GENE MUTATION; HOMOZYGOTE; MALE; MOUSE; NEWBORN; NONHUMAN; OBESITY; PHENOTYPE; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA DEGENERATION; SPERMATOCYTE;

ABNORMALITIES, MULTIPLE; ANIMALS; DEAFNESS; HUMANS; MALE; MICE; MICE, INBRED C57BL; MICE, MUTANT STRAINS; OBESITY; PHOTORECEPTORS; PROTEINS; RETINAL DEGENERATION; RETINITIS PIGMENTOSA; SPERM COUNT; SPERM MOTILITY; SPERMATOZOA; SYNDROME;

ANIMALIA; MURINAE;

EID: 0031904993     PISSN: 0302766X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004410051018     Document Type: Article

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