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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2003 | 1 |
2007 | 1 |
2024 | 0 |
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3 results
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Page 1
Mutations in a Sar1 GTPase of COPII vesicles are associated with lipid absorption disorders.
Nat Genet. 2003 May;34(1):29-31. doi: 10.1038/ng1145.
Nat Genet. 2003.
PMID: 12692552
SIL1 and SARA2 mutations in Marinesco-Sjögren and chylomicron retention diseases.
Annesi G, Aguglia U, Tarantino P, Annesi F, De Marco EV, Civitelli D, Torroni A, Quattrone A.
Annesi G, et al.
Clin Genet. 2007 Mar;71(3):288-9. doi: 10.1111/j.1399-0004.2007.00759.x.
Clin Genet. 2007.
PMID: 17309654
No abstract available.
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Vitamin E deficiency due to chylomicron retention disease in Marinesco-Sjögren syndrome.
Aguglia U, Annesi G, Pasquinelli G, Spadafora P, Gambardella A, Annesi F, Pasqua AA, Cavalcanti F, Crescibene L, Bagalà A, Bono F, Oliveri RL, Valentino P, Zappia M, Quattrone A.
Aguglia U, et al.
Ann Neurol. 2000 Feb;47(2):260-4.
Ann Neurol. 2000.
PMID: 10665502
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