SPECC1L regulates palate development downstream of IRF6
Everett G. Hall, Luke W. Wenger, Nathan R. Wilson, Sraavya S Undurty-Akella et autres
SPECC1L mutations have been identified in patients with rare atypical orofacial clefts and with syndromic cleft lip and/or palate (CL/P). These mutations cluster in the second coiled-coil and calponin homology domains of SPECC1L and severely affect the ability of SPECC1L to associate …
us, jp, Nigéria, Éthiopie (code pays fourni par la source)
27 citations
Human Molecular Genetics