De Novo Mutations From Sporadic Schizophrenia Cases Highlight Important Signaling Genes in an Independent Sample

Schizophrenia Research - Netherlands
doi 10.1016/j.schres.2015.05.042
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Elsevier BV

Related search

De Novo Mutations in Sporadic Deletional Duchenne Muscular Dystrophy (DMD) Cases

Experimental & Molecular Medicine
2003English

Sporadic Hypertrophic Cardiomyopathy Due to De Novo Myosin Mutations.

Journal of Clinical Investigation
Medicine
1992English

Exome Sequencing to Identify De Novo Mutations in Sporadic ALS Trios

Nature Neuroscience
Neuroscience
2013English

Three Novel F8 Mutations in Sporadic Haemophilia a Cases

SpringerPlus
Multidisciplinary
2012English

Recurrent De Novo Mutations Implicate Novel Genes Underlying Simplex Autism Risk

Nature Communications
AstronomyGeneticsMolecular BiologyBiochemistryChemistryPhysics
2014English

Genes With De Novo Mutations Are Shared by Four Neuropsychiatric Disorders Discovered From NPdenovo Database

Molecular Psychiatry
PsychiatryMolecular NeuroscienceMental HealthMolecular BiologyCellular
2015English

De Novo Mutations in FOXP1 in Cases With Intellectual Disability, Autism, and Language Impairment

American Journal of Human Genetics
Genetics
2010English

De Novo Mutations in the Gene Encoding the Synaptic Scaffolding proteinSHANK3in Patients Ascertained for Schizophrenia

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2010English

Two Novel Large ANKH Deletion Mutations in Sporadic Cases With Craniometaphyseal Dysplasia

Clinical Genetics
Genetics
2011English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy