A CTNNA3 compound heterozygous deletion implicates a role for αT-catenin in susceptibility to autism spectrum disorder
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D. Pinto | E. Bacchelli | A. Battaglia | E. Maestrini | R. Tancredi | E. Bonora | P. D’Adamo | Piero Parchi | Maila Giannandrea | F. Ceroni | Silvia Lomartire | Fabiola Ceroni