Frontiers | De novo mutations, genetic mosaicism and human disease
Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation - ScienceDirect
Genes | Free Full-Text | Somatic Mosaicism in the Human Genome
Types of sporadic gene mutations leading to disease. (a, b) De novo... | Download Scientific Diagram
Can De novo genetic mutations give rise to Brain disorders like Autism? - Biomall Blog
What is a de novo mutation? Find out below! | By SPARK for AutismFacebook
Inheritance – Bohring-Opitz Syndrome
De Novo” Mutations in Dozens of Genes Cause Autism : Bipolar Network News
De novo mutations in schizophrenia implicate synaptic networks | Nature
De novo mutations in folate-related genes associated with common developmental disorders - ScienceDirect
The role of de novo mutations in adult-onset neurodegenerative disorders | Acta Neuropathologica
When bestrophinopathies don't run in the family? | UCL Institute of Ophthalmology - UCL – University College London
De Novo Mutations Reflect Development and Aging of the Human Germline: Trends in Genetics
Frontiers | De novo mutations, genetic mosaicism and human disease
denovo-DB
De novo mutations in human genetic disease | Nature Reviews Genetics
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder | Science
De novo mutation in NALCN. A: Pictures of the patient and of one of her... | Download Scientific Diagram
Finding the difference: de novo mutations in schizophrenia | Beyond the Ion Channel
A de novo mutation in the NALCN gene in an adult patient with cerebellar ataxia associated with intellectual disability and arthrogryposis - Wang - 2016 - Clinical Genetics - Wiley Online Library
![PDF] De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/0b264bac49270d7d896e6d7fd3a1b3db7daec8f2/7-Figure2-1.png "PDF] De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene | Semantic Scholar")
PDF] De novo mutation screening in childhood-onset cerebellar atrophy identifies gain-of-function mutations in the CACNA1G calcium channel gene | Semantic Scholar
New insights into the generation and role of de novo mutations in health and disease | Genome Biology | Full Text
Epileptic encephalopathies: de novo mutations take center stage | Beyond the Ion Channel
TADA – a joint analysis of de novo and inherited risk factors in autism | Beyond the Ion Channel
De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia | Semantic Scholar
De novo mutations in human genetic disease | Nature Reviews Genetics
