De novo mutations in human genetic disease | Nature Reviews Genetics
![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
Autism study finds de novo mutations associated with motor skill deficiencies
De novo gene birth - Wikipedia
Finding the difference: de novo mutations in schizophrenia | Beyond the Ion Channel
De Novo Synonymous Mutations in Regulatory Elements Contribute to the Genetic Etiology of Autism and Schizophrenia | Semantic Scholar
What is a de novo mutation? Find out below! | By SPARK for AutismFacebook
Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder | Science
Epileptic encephalopathies: de novo mutations take center stage | Beyond the Ion Channel
Frontiers | De novo mutations, genetic mosaicism and human disease
De novo mutations in isolated RP patients. A: De novo m | Open-i
De novo - Definition and Examples | Biology Online
Can De novo genetic mutations give rise to Brain disorders like Autism? - Biomall Blog
The role of de novo mutations in adult-onset neurodegenerative disorders | Acta Neuropathologica
New insights into the generation and role of de novo mutations in health and disease | Genome Biology | Full Text
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
Types of sporadic gene mutations leading to disease. (a, b) De novo... | Download Scientific Diagram
Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation - ScienceDirect
De Novo Mutations Reflect Development and Aging of the Human Germline: Trends in Genetics
De novo mutations in folate-related genes associated with common developmental disorders - ScienceDirect
NEJM on X: "De novo mutation — Any DNA sequence change that occurs during replication, such as a gene alteration newly occurring in a family as a result of a DNA sequence
Hereditary spherocytosis: Genetics
SFARI | Meta-analysis of de novo mutations yields longer list of risk genes for neurodevelopmental disorders
