RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism-Reference-Cited by-同舟云学术

RB1CC1 duplication and aberrant overexpression in a patient with schizophrenia: further phenotype delineation and proposal of a pathogenetic mechanism

Published:2020-12-19 Issue:1 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Errichiello Edoardo¹^ORCID,Giorda Roberto²^ORCID,Gambale Antonella³⁴^ORCID,Iolascon Achille³⁴^ORCID,Zuffardi Orsetta¹^ORCID,Giglio Sabrina⁵^ORCID

Affiliation:

1. Unit of Medical Genetics Department of Molecular Medicine University of Pavia Pavia Italy

2. Laboratory of Molecular Biology Scientific Institute IRCCS Eugenio Medea Bosisio Parini Italy

3. Department of Molecular Medicine and Medical Biotechnologies University "Federico II" of Naples Naples Italy

4. CEINGE, Advanced Biotechnologies Naples Italy

5. Unit of Medical Genetics, Department of Medical Sciences and Public Health University of Cagliari Cagliari Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1561

Reference42 articles.

1. Regulation of Focal Adhesion Kinase by a Novel Protein Inhibitor FIP200

2. Exome sequence analysis and follow up genotyping implicates rare ULK1 variants to be involved in susceptibility to schizophrenia

3. Disrupted in Schizophrenia 1 forms pathological aggresomes that disrupt its function in intracellular transport

4. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome

5. Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients

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