A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene | European Journal of Human Genetics
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
Frontiers | Rare diseases of epigenetic origin: Challenges and opportunities
ATPase SRCAP is a new player in cell division, uncovering molecular aspects of Floating-Harbor syndrome | bioRxiv
SRCAP siRNA (h), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
ATPase SRCAP is a new player in cell division, uncovering molecular aspects of Floating-Harbor syndrome | bioRxiv
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
Severe developmental expressive language disorder due to a frameshift mutation in exon 18 of SRCAP gene, far away from the mutational hotspot in exons 33 and 34 associated to the Floating-Harbor syndrome | SpringerLink
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
Schematic representation of the SRCAP gene and positions of known SRCAP... | Download Scientific Diagram
JDB | Free Full-Text | The Role of the Histone Variant H2A.Z in Metazoan Development
The chromatin remodeler SRCAP promotes self‐renewal of intestinal stem cells | The EMBO Journal
A schematic structure of the SRCAP gene and the locations of mutations... | Download Scientific Diagram
A schematic of the SRCAP gene and comparison of SRCAP-conserved ATPase... | Download Scientific Diagram
Adenovirus DNA Binding Protein Interacts with the SNF2-Related CBP Activator Protein (SrCap) and Inhibits SrCap-Mediated Transcription | Journal of Virology
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
Engineered FHS SRCAP heterozygous human CNCCs show downregulation of... | Download Scientific Diagram
Cryo-EM structure of human SRCAP complex | Cell Research
![PDF] Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome. | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/54b6e928b2ee7b886ac951adbac98bc7334fc800/5-Figure2-1.png "PDF] Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome. | Semantic Scholar")
PDF] Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndrome. | Semantic Scholar
Gene Reactivation by 5-Aza-2′-Deoxycytidine–Induced Demethylation Requires SRCAP–Mediated H2A.Z Insertion to Establish Nucleosome Depleted Regions | PLOS Genetics
The SRCAP chromatin remodeling complex promotes oxidative metabolism during prenatal heart development
When chromatin organisation floats astray: the Srcap gene and Floating–Harbor syndrome
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome | BMC Medical Genetics | Full Text
