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Year | Number of Results |
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1991 | 1 |
1993 | 2 |
2024 | 0 |
PubMed for id: 220073
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De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III).
Nat Genet. 1993 Nov;5(3):266-8. doi: 10.1038/ng1193-266.
Nat Genet. 1993.
PMID: 7506095
Structure and chromosomal localization of the gene encoding the human myelin protein zero (MPZ).
Hayasaka K, Himoro M, Wang Y, Takata M, Minoshima S, Shimizu N, Miura M, Uyemura K, Takada G.
Hayasaka K, et al.
Genomics. 1993 Sep;17(3):755-8. doi: 10.1006/geno.1993.1400.
Genomics. 1993.
PMID: 7503936
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Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin.
Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, Uyemura K.
Hayasaka K, et al.
Biochem Biophys Res Commun. 1991 Oct 31;180(2):515-8. doi: 10.1016/s0006-291x(05)81094-0.
Biochem Biophys Res Commun. 1991.
PMID: 1719967
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