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Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome
Yeh E,
Fanganiello RD,
Sunaga DY,
Zhou X,
Holmes G,
et al.
(2013)
Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome.
PLOS ONE 8(4): e60439.
https://doi.org/10.1371/journal.pone.0060439