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Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype-phenotype associations for laminopathies

✍ Scribed by Scharner, Juergen; Lu, Hui-Chun; Fraternali, Franca; Ellis, Juliet A.; Zammit, Peter S.


Book ID
121838024
Publisher
John Wiley and Sons
Year
2013
Tongue
English
Weight
515 KB
Volume
82
Category
Article
ISSN
0887-3585

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