Missense mutations in FBN1...

American Journal of Medical Genetics Part A 2013 / 09 Vol. 161; Iss. 9

Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome

Cecchi, Alana, Ogawa, Naomi, Martinez, Hugo R., Carlson, Alicia, Fan, Yuxin, Penny, Daniel J., Guo, Dong-chuan, Eisenberg, Steven, Safi, Hazim, Estrera, Anthony, Lewis, Richard A., Meyers, Deborah, Mi
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Volume:
161
Language:
english
Journal:
American Journal of Medical Genetics Part A
DOI:
10.1002/ajmg.a.36044
Date:
September, 2013
File:
PDF, 374 KB
english, 2013
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