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Giant axonal neuropathy caused by compound heterozygosity for a maternally inherited microdeletion and a paternal mutation within the GAN gene

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Keywords
GIGAXONIN, giant axonal neuropathy, GENOTYPE-PHENOTYPE, GAN, gigaxonin, array CGH, 16q23.2 microdeletion

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Citation

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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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