Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene
- Author
- Karen Buysse (UGent) , Sarah Vergult (UGent) , Silke Mussche (UGent) , Chantal Ceuterick-De Groote, Franki Speleman (UGent) , Björn Menten (UGent) , Willy Lissens and Rudy Van Coster (UGent)
- Organization
- Keywords
- GIGAXONIN, giant axonal neuropathy, GENOTYPE-PHENOTYPE, GAN, gigaxonin, array CGH, 16q23.2 microdeletion
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-1071781
- MLA
- Buysse, Karen, et al. “Giant Axonal Neuropathy Caused by Compound Heterozygosity for a Maternally Inherited Microdeletion and a Paternal Mutation within the GAN Gene.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol. 152A, no. 11, 2010, pp. 2802–04, doi:10.1002/ajmg.a.33508.
- APA
- Buysse, K., Vergult, S., Mussche, S., Ceuterick-De Groote, C., Speleman, F., Menten, B., … Van Coster, R. (2010). Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 152A(11), 2802–2804. https://doi.org/10.1002/ajmg.a.33508
- Chicago author-date
- Buysse, Karen, Sarah Vergult, Silke Mussche, Chantal Ceuterick-De Groote, Franki Speleman, Björn Menten, Willy Lissens, and Rudy Van Coster. 2010. “Giant Axonal Neuropathy Caused by Compound Heterozygosity for a Maternally Inherited Microdeletion and a Paternal Mutation within the GAN Gene.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 152A (11): 2802–4. https://doi.org/10.1002/ajmg.a.33508.
- Chicago author-date (all authors)
- Buysse, Karen, Sarah Vergult, Silke Mussche, Chantal Ceuterick-De Groote, Franki Speleman, Björn Menten, Willy Lissens, and Rudy Van Coster. 2010. “Giant Axonal Neuropathy Caused by Compound Heterozygosity for a Maternally Inherited Microdeletion and a Paternal Mutation within the GAN Gene.” AMERICAN JOURNAL OF MEDICAL GENETICS PART A 152A (11): 2802–2804. doi:10.1002/ajmg.a.33508.
- Vancouver
- 1.Buysse K, Vergult S, Mussche S, Ceuterick-De Groote C, Speleman F, Menten B, et al. Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010;152A(11):2802–4.
- IEEE
- [1]K. Buysse et al., “Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene,” AMERICAN JOURNAL OF MEDICAL GENETICS PART A, vol. 152A, no. 11, pp. 2802–2804, 2010.
@article{1071781, author = {{Buysse, Karen and Vergult, Sarah and Mussche, Silke and Ceuterick-De Groote, Chantal and Speleman, Franki and Menten, Björn and Lissens, Willy and Van Coster, Rudy}}, issn = {{1552-4825}}, journal = {{AMERICAN JOURNAL OF MEDICAL GENETICS PART A}}, keywords = {{GIGAXONIN,giant axonal neuropathy,GENOTYPE-PHENOTYPE,GAN,gigaxonin,array CGH,16q23.2 microdeletion}}, language = {{eng}}, number = {{11}}, pages = {{2802--2804}}, title = {{Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene}}, url = {{http://doi.org/10.1002/ajmg.a.33508}}, volume = {{152A}}, year = {{2010}}, }
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