has been cited by the following article(s):
[1]
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De novo heterozygousFBN1mutations in the extreme C-terminal region cause progeroid fibrillinopathy
American Journal of Medical Genetics Part A,
2014
DOI:10.1002/ajmg.a.36449
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[2]
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De novo heterozygous FBN1 mutations in the extreme C‐terminal region cause progeroid fibrillinopathy
American Journal of Medical Genetics Part A,
2014
DOI:10.1002/ajmg.a.36449
|
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