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JMG.37.12.E41
JMG.37.12.E41
http://dx.doi.org/10.1136/JMG.37.12.E41
Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome.
P356
Q43076197-21A58460-CD5C-4FDE-A4EC-7A3FCC5C6DFD
P356
JMG.37.12.E41
http://dx.doi.org/10.1136/JMG.37.12.E41