Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature - ScienceDirect
The chromatin remodeler SRCAP promotes self‐renewal of intestinal stem cells | The EMBO Journal
When chromatin organisation floats astray: the Srcap gene and Floating–Harbor syndrome
Gene Reactivation by 5-Aza-2′-Deoxycytidine–Induced Demethylation Requires SRCAP–Mediated H2A.Z Insertion to Establish Nucleosome Depleted Regions | PLOS Genetics
ATPase SRCAP is a new player in cell division, uncovering molecular aspects of Floating-Harbor syndrome | bioRxiv
Frontiers | Rare diseases of epigenetic origin: Challenges and opportunities
A neurodevelopmental disorder caused by a novel de novo SVA insertion in exon 13 of the SRCAP gene | European Journal of Human Genetics
Cryo-EM structure of human SRCAP complex | Cell Research
JDB | Free Full-Text | The Role of the Histone Variant H2A.Z in Metazoan Development
Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specifi
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
A schematic structure of the SRCAP gene and the locations of mutations... | Download Scientific Diagram
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
Addgene: Mouse 5' Srcap AID GFP Puro
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
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
A schematic of the SRCAP gene and comparison of SRCAP-conserved ATPase... | Download Scientific Diagram
Schematic representation of the SRCAP gene and positions of known SRCAP... | Download Scientific Diagram
Research – Boyer Labs
SRCAP Gene - GeneCards | SRCAP Protein | SRCAP Antibody
The Human SRCAP Chromatin Remodeling Complex Promotes DNA-End Resection - ScienceDirect
ATPase SRCAP is a new player in cell division, uncovering molecular aspects of Floating-Harbor syndrome | bioRxiv
Schematic representation of the SRCAP gene and positions of known SRCAP... | Download Scientific Diagram
Single Amino Acid Change Underlies Distinct Roles of H2A.Z Subtypes in Human Syndrome
The ATPase SRCAP is associated with the mitotic apparatus, uncovering novel molecular aspects of Floating-Harbor syndrome | BMC Biology | Full Text
Engineered FHS SRCAP heterozygous human CNCCs show downregulation of... | Download Scientific Diagram
![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
