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De novo heterozygous FBN1 mutations in the extreme C‐terminal region cause progeroid fibrillinopathy
Author(s) -
Garg Abhimanyu,
Xing Chao
Publication year - 2014
Publication title -
american journal of medical genetics part a
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 1.064
H-Index - 112
eISSN - 1552-4833
pISSN - 1552-4825
DOI - 10.1002/ajmg.a.36449
Subject(s) - center (category theory) , library science , gerontology , medicine , computer science , crystallography , chemistry