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Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice
Vissers LELM,
Cox TC,
Maga AM,
Short KM,
Wiradjaja F,
et al.
(2011)
Heterozygous Mutations of FREM1 Are Associated with an Increased Risk of Isolated Metopic Craniosynostosis in Humans and Mice.
PLOS Genetics 7(9): e1002278.
https://doi.org/10.1371/journal.pgen.1002278