No Evidence for Rare Recessive and Compound Heterozygous Disruptive Variants in Schizophrenia

European Journal of Human Genetics - United Kingdom
doi 10.1038/ejhg.2014.228
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Epileptic Encephalopathy and Cerebellar Atrophy Resulting From Compound Heterozygous CACNA2D2 Variants

Case Reports in Genetics
2018English

Compound Heterozygous SPATA5 Variants in Four Families and Functional Studies of SPATA5 Deficiency

European Journal of Human Genetics
Genetics
2018English

Compound Heterozygous Novel Frameshift Variants in the PROM1 Gene Result in Leber Congenital Amaurosis

Cold Spring Harbor molecular case studies
BiochemistryMolecular MedicineGenetics
2019English

Association of Common and Rare Genetic Variants With Cognition in Schizophrenia

Canadian Journal of Biotechnology
2017English

Familial Dilated Cardiomyopathy Associated With a Novel Combination of Compound Heterozygous TNNC1 Variants

Frontiers in Physiology
Physiology
2020English

Novel Compound Heterozygous TMEM67 Variants in a Vietnamese Family With Joubert Syndrome: A Case Report

BMC Medical Genetics
Genetics
2020English

Discovery of Rare Variants Implicated in Schizophrenia Using Next-Generation Sequencing

Journal of Translational Genetics and Genomics
2019English

HbA1c Levels in Individuals Heterozygous for Hemoglobin Variants

Revista da Associacao Medica Brasileira
Medicine
2017English

Compound Heterozygous NEK1 Variants in Two Siblings With Oral-Facial-Digital Syndrome Type II (Mohr Syndrome)

European Journal of Human Genetics
Genetics
2016English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy