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Year | Number of Results |
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2008 | 1 |
2010 | 1 |
2024 | 0 |
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Mutations in fibrillin-1 cause congenital scleroderma: stiff skin syndrome.
Sci Transl Med. 2010 Mar 17;2(23):23ra20. doi: 10.1126/scitranslmed.3000488.
Sci Transl Med. 2010.
PMID: 20375004
Free PMC article.
Fibrillin-integrin interactions in health and disease.
Jovanović J, Iqbal S, Jensen S, Mardon H, Handford P.
Jovanović J, et al.
Biochem Soc Trans. 2008 Apr;36(Pt 2):257-62. doi: 10.1042/BST0360257.
Biochem Soc Trans. 2008.
PMID: 18363569
Review.
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