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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1996 | 2 |
2000 | 1 |
2024 | 0 |
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Page 1
Analysis of the structure and function of the von Willebrand factor A1 domain using targeted deletions and alanine-scanning mutagenesis.
Biochemistry. 1996 Oct 15;35(41):13460-8. doi: 10.1021/bi9610313.
Biochemistry. 1996.
PMID: 8873615
The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor.
Kroner PA, Foster PA, Fahs SA, Montgomery RR.
Kroner PA, et al.
Blood. 1996 Feb 1;87(3):1013-21.
Blood. 1996.
PMID: 8562925
Free article.
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The human multimerin gene MMRN maps to chromosome 4q22.
Torres MD, Van Tuinen P, Kroner PA.
Torres MD, et al.
Cytogenet Cell Genet. 2000;88(3-4):275-7. doi: 10.1159/000015537.
Cytogenet Cell Genet. 2000.
PMID: 10828608
No abstract available.
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