Shank3 deletion in PV neurons is associated with abnormal behaviors and neuronal functions that are rescued by increasing GABAergic signaling

[1] Bonaglia MC(2001)Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q133 deletion syndrome Am J Hum Genet 69 261-268

[2] Giorda R(2022)Phelan-McDermid syndrome: a classification system after 30 years of experience Orphanet J Rare Dis 17 27-201

[3] Borgatti R(2012)The 22q13.3 deletion syndrome (Phelan-McDermid syndrome) Mol Syndromol. 2 186-99

[4] Felisari G(2001)22q13 deletion syndrome Am J Med Genet 101 91-328

[5] Gagliardi C(2014)22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndrome Genet Med 16 318-84

[6] Selicorni A(2012)SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism Mol Psychiatry 17 71-27

[7] Phelan K(2014)Meta-analysis of SHANK mutations in autism spectrum disorders: a gradient of severity in cognitive impairments PLoS Genet 10 25-61

[8] Boccuto L(2007)Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders Nat Genet 39 45-120

[9] Powell CM(2011)Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons Dev Neurobiol 71 107-349

[10] Boeckers TM(2012)Interneuron dysfunction in psychiatric disorders Nat Rev Neurosci 13 343-1583

[1] Bonaglia MC(2001)Disruption of the ProSAP2 gene in a t(12;22)(q24.1;q13.3) is associated with the 22q133 deletion syndrome Am J Hum Genet 69 261-268

[2] Giorda R(2022)Phelan-McDermid syndrome: a classification system after 30 years of experience Orphanet J Rare Dis 17 27-201

[3] Borgatti R(2012)The 22q13.3 deletion syndrome (Phelan-McDermid syndrome) Mol Syndromol. 2 186-99

[4] Felisari G(2001)22q13 deletion syndrome Am J Med Genet 101 91-328

[5] Gagliardi C(2014)22q13.2q13.32 genomic regions associated with severity of speech delay, developmental delay, and physical features in Phelan-McDermid syndrome Genet Med 16 318-84

[6] Selicorni A(2012)SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism Mol Psychiatry 17 71-27

[7] Phelan K(2014)Meta-analysis of SHANK mutations in autism spectrum disorders: a gradient of severity in cognitive impairments PLoS Genet 10 25-61

[8] Boccuto L(2007)Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders Nat Genet 39 45-120

[9] Powell CM(2011)Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons Dev Neurobiol 71 107-349

[10] Boeckers TM(2012)Interneuron dysfunction in psychiatric disorders Nat Rev Neurosci 13 343-1583