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Year | Number of Results |
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1996 | 1 |
2002 | 1 |
2003 | 1 |
2024 | 0 |
PubMed for id: 37790789
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Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy.
Am J Hum Genet. 2003 Nov;73(5):1106-19. doi: 10.1086/379525. Epub 2003 Oct 21.
Am J Hum Genet. 2003.
PMID: 14574644
Free PMC article.
HUGE: a database for human large proteins identified in the Kazusa cDNA sequencing project.
Kikuno R, Nagase T, Waki M, Ohara O.
Kikuno R, et al.
Nucleic Acids Res. 2002 Jan 1;30(1):166-8. doi: 10.1093/nar/30.1.166.
Nucleic Acids Res. 2002.
PMID: 11752282
Free PMC article.
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Homozygosity mapping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33.
LeGuern E, Guilbot A, Kessali M, Ravisé N, Tassin J, Maisonobe T, Grid D, Brice A.
LeGuern E, et al.
Hum Mol Genet. 1996 Oct;5(10):1685-8. doi: 10.1093/hmg/5.10.1685.
Hum Mol Genet. 1996.
PMID: 8894708
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