[CITATION][C] MEF2C mutations are a rare cause of Rett or severe Rett‐like encephalopathies
L Lambert, T Bienvenu, L Allou, M Valduga… - Clinical …, 2012 - Wiley Online Library
L Lambert, T Bienvenu, L Allou, M Valduga, B Echenne, B Diebold, C Mignot, D Héron…
Clinical genetics, 2012•Wiley Online LibraryRett syndrome (RTT) is clinically and genetically heterogeneous with three genes (MECP2,
CDKL5 and FOXG1) clearly implicated in these neurological disorders. However, some
patients with classic RTT and even more with atypical RTT are still waiting for a genetic
diagnosis. Recently, the MEF2C gene was
CDKL5 and FOXG1) clearly implicated in these neurological disorders. However, some
patients with classic RTT and even more with atypical RTT are still waiting for a genetic
diagnosis. Recently, the MEF2C gene was
Rett syndrome (RTT) is clinically and genetically heterogeneous with three genes (MECP2, CDKL5 and FOXG1) clearly implicated in these neurological disorders. However, some patients with classic RTT and even more with atypical RTT are still waiting for a genetic diagnosis. Recently, the MEF2C gene was
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