https://www.selleckchem.com/Proteasome.html
1026C G (C342W) in exon 10 of FGFR2 in both the patient and his mother, but not in any of the unaffected family members. None. Our study confirms the presence of optic nerve atrophy in patients with Crouzon syndrome carrying FGFR2 C342W mutations and indicates that MRI and funduscopy should be performed to examine the optic nerve changes for patients with Crouzon syndrome. Our study confirms the presence of optic nerve atrophy in patients with Crouzon syndrome carrying FGFR2 C342W mutations and indicates that MRI and funduscopy should be
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