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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2003 | 1 |
2009 | 1 |
2010 | 1 |
2015 | 1 |
2016 | 1 |
2019 | 1 |
2021 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 5192
7 results
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Page 1
Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort.
Andrology. 2021 Jul;9(4):1151-1165. doi: 10.1111/andr.13009. Epub 2021 Apr 20.
Andrology. 2021.
PMID: 33784440
Free article.
PEX10, SIRPA-SIRPG, and SOX5 gene polymorphisms are strongly associated with nonobstructive azoospermia susceptibility.
Gu X, Li H, Chen X, Zhang X, Mei F, Jia M, Xiong C.
Gu X, et al.
J Assist Reprod Genet. 2019 Apr;36(4):759-768. doi: 10.1007/s10815-019-01417-w. Epub 2019 Mar 13.
J Assist Reprod Genet. 2019.
PMID: 30863997
Free PMC article.
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Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.
Renaud M, Guissart C, Mallaret M, Ferdinandusse S, Cheillan D, Drouot N, Muller J, Claustres M, Tranchant C, Anheim M, Koenig M.
Renaud M, et al.
J Neurol. 2016 Aug;263(8):1552-8. doi: 10.1007/s00415-016-8167-3. Epub 2016 May 26.
J Neurol. 2016.
PMID: 27230853
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[Abnormal expression of PEX10 gene may be related to epilepsy associated with 1p36 copy number variations].
Zhang Y, Xu F, Tan Y, Hu J, Wang H.
Zhang Y, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015 Feb;32(1):6-10. doi: 10.3760/cma.j.issn.1003-9406.2015.01.002.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2015.
PMID: 25636090
Chinese.
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Mutations in PEX10 are a cause of autosomal recessive ataxia.
Régal L, Ebberink MS, Goemans N, Wanders RJ, De Meirleir L, Jaeken J, Schrooten M, Van Coster R, Waterham HR.
Régal L, et al.
Ann Neurol. 2010 Aug;68(2):259-63. doi: 10.1002/ana.22035.
Ann Neurol. 2010.
PMID: 20695019
Review.
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Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
Yik WY, Steinberg SJ, Moser AB, Moser HW, Hacia JG.
Yik WY, et al.
Hum Mutat. 2009 Mar;30(3):E467-80. doi: 10.1002/humu.20932.
Hum Mutat. 2009.
PMID: 19105186
Free PMC article.
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Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.
Shimozawa N, Nagase T, Takemoto Y, Suzuki Y, Kondo N.
Shimozawa N, et al.
Adv Exp Med Biol. 2003;544:71. doi: 10.1007/978-1-4419-9072-3_10.
Adv Exp Med Biol. 2003.
PMID: 14713216
No abstract available.
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