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The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

(2003) HISTOCHEMISTRY AND CELL BIOLOGY. 119(3). p.247-256
Author
Organization
Keywords
LOCALIZATION, COCHLEA, ENDOPLASMIC-RETICULUM, VESTIBULAR HAIR-CELLS, GUINEA-PIG, CANALICULAR RETICULUM, TRANSMEMBRANE PROTEIN, DIABETES-MELLITUS, CA2+ RELEASE, OPTIC ATROPHY

Citation

Please use this url to cite or link to this publication:

MLA
Cryns, K et al. “The WFS1 Gene, Responsible for Low Frequency Sensorineural Hearing Loss and Wolfram Syndrome, Is Expressed in a Variety of Inner Ear Cells.” HISTOCHEMISTRY AND CELL BIOLOGY 119.3 (2003): 247–256. Print.
APA
Cryns, K., Thys, S., Van Laer, L., Oka, Y., Pfister, M., Van Nassauw, L., Smith, R., et al. (2003). The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. HISTOCHEMISTRY AND CELL BIOLOGY, 119(3), 247–256.
Chicago author-date
Cryns, K, S Thys, Lut Van Laer, Y Oka, M Pfister, L Van Nassauw, RJH Smith, JP Timmermans, and G Van Camp. 2003. “The WFS1 Gene, Responsible for Low Frequency Sensorineural Hearing Loss and Wolfram Syndrome, Is Expressed in a Variety of Inner Ear Cells.” Histochemistry and Cell Biology 119 (3): 247–256.
Chicago author-date (all authors)
Cryns, K, S Thys, Lut Van Laer, Y Oka, M Pfister, L Van Nassauw, RJH Smith, JP Timmermans, and G Van Camp. 2003. “The WFS1 Gene, Responsible for Low Frequency Sensorineural Hearing Loss and Wolfram Syndrome, Is Expressed in a Variety of Inner Ear Cells.” Histochemistry and Cell Biology 119 (3): 247–256.
Vancouver
1.
Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, et al. The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. HISTOCHEMISTRY AND CELL BIOLOGY. NEW YORK: SPRINGER-VERLAG; 2003;119(3):247–56.
IEEE
[1]
K. Cryns et al., “The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells,” HISTOCHEMISTRY AND CELL BIOLOGY, vol. 119, no. 3, pp. 247–256, 2003.
@article{801405,
  author       = {{Cryns, K and Thys, S and Van Laer, Lut and Oka, Y and Pfister, M and Van Nassauw, L and Smith, RJH and Timmermans, JP and Van Camp, G}},
  issn         = {{0948-6143}},
  journal      = {{HISTOCHEMISTRY AND CELL BIOLOGY}},
  keywords     = {{LOCALIZATION,COCHLEA,ENDOPLASMIC-RETICULUM,VESTIBULAR HAIR-CELLS,GUINEA-PIG,CANALICULAR RETICULUM,TRANSMEMBRANE PROTEIN,DIABETES-MELLITUS,CA2+ RELEASE,OPTIC ATROPHY}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{247--256}},
  publisher    = {{SPRINGER-VERLAG}},
  title        = {{The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells}},
  url          = {{http://dx.doi.org/10.1007/s00418-003-0495-6}},
  volume       = {{119}},
  year         = {{2003}},
}

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