A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.
- Author
- A RAAS-ROTHSCHILD, R WANDERS, P MOOIJER, J GOOTJES, HR WATERHAM, A GUTMAN, Y SUZUKI, N SHIMOZAWA, N KONDO, G ESHEL, Marc Espeel (UGent) , Frank Roels (UGent) and SH KORMAN
- Organization
Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-150208
- MLA
- RAAS-ROTHSCHILD, A., et al. “A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents.” AMERICAN JOURNAL OF HUMAN GENETICS, vol. 70, no. 4, 2002, pp. 1062–68.
- APA
- RAAS-ROTHSCHILD, A., WANDERS, R., MOOIJER, P., GOOTJES, J., WATERHAM, H., GUTMAN, A., … KORMAN, S. (2002). A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents. AMERICAN JOURNAL OF HUMAN GENETICS, 70(4), 1062–1068.
- Chicago author-date
- RAAS-ROTHSCHILD, A, R WANDERS, P MOOIJER, J GOOTJES, HR WATERHAM, A GUTMAN, Y SUZUKI, et al. 2002. “A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents.” AMERICAN JOURNAL OF HUMAN GENETICS 70 (4): 1062–68.
- Chicago author-date (all authors)
- RAAS-ROTHSCHILD, A, R WANDERS, P MOOIJER, J GOOTJES, HR WATERHAM, A GUTMAN, Y SUZUKI, N SHIMOZAWA, N KONDO, G ESHEL, Marc Espeel, Frank Roels, and SH KORMAN. 2002. “A PEX6-Defective Peroxisomal Biogenesis Disorder with Severe Phenotype in an Infant, versus Mild Phenotype Resembling Usher Syndrome in the Affected Parents.” AMERICAN JOURNAL OF HUMAN GENETICS 70 (4): 1062–1068.
- Vancouver
- 1.RAAS-ROTHSCHILD A, WANDERS R, MOOIJER P, GOOTJES J, WATERHAM H, GUTMAN A, et al. A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents. AMERICAN JOURNAL OF HUMAN GENETICS. 2002;70(4):1062–8.
- IEEE
- [1]A. RAAS-ROTHSCHILD et al., “A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.,” AMERICAN JOURNAL OF HUMAN GENETICS, vol. 70, no. 4, pp. 1062–1068, 2002.
@article{150208,
author = {{RAAS-ROTHSCHILD, A and WANDERS, R and MOOIJER, P and GOOTJES, J and WATERHAM, HR and GUTMAN, A and SUZUKI, Y and SHIMOZAWA, N and KONDO, N and ESHEL, G and Espeel, Marc and Roels, Frank and KORMAN, SH}},
issn = {{0002-9297}},
journal = {{AMERICAN JOURNAL OF HUMAN GENETICS}},
language = {{eng}},
number = {{4}},
pages = {{1062--1068}},
title = {{A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.}},
volume = {{70}},
year = {{2002}},
}