![A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text](https://media.springernature.com/lw685/springer-static/image/art%3A10.1186%2Fs12944-019-1181-6/MediaObjects/12944_2019_1181_Fig4_HTML.png)
A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text
![The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs42255-019-0138-4/MediaObjects/42255_2019_138_Fig1_HTML.png)
The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
![By Stephen Monahan. Genes on chromosome 3 include ABHD5,ALAS1, AMT,ATP2B2, and BCHE Chromosome 3 contains between 1,100 to 1,500 genes where ABHD5,ALAS1, - ppt download By Stephen Monahan. Genes on chromosome 3 include ABHD5,ALAS1, AMT,ATP2B2, and BCHE Chromosome 3 contains between 1,100 to 1,500 genes where ABHD5,ALAS1, - ppt download](https://images.slideplayer.com/23/6569502/slides/slide_5.jpg)
By Stephen Monahan. Genes on chromosome 3 include ABHD5,ALAS1, AMT,ATP2B2, and BCHE Chromosome 3 contains between 1,100 to 1,500 genes where ABHD5,ALAS1, - ppt download
![Genes | Free Full-Text | Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome Genes | Free Full-Text | Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome](https://www.mdpi.com/genes/genes-12-01164/article_deploy/html/images/genes-12-01164-g002.png)
Genes | Free Full-Text | Maternal Isodisomy of Chromosome 3 Combined with a De Novo Mutation in the ABHD5 Gene Causes Autosomal Recessive Chanarin-Dorfman Syndrome
![ABHD5 protein structure and function. Schematic representation of ABHD5... | Download Scientific Diagram ABHD5 protein structure and function. Schematic representation of ABHD5... | Download Scientific Diagram](https://www.researchgate.net/publication/338222320/figure/fig1/AS:841419002503169@1577621331195/ABHD5-protein-structure-and-function-Schematic-representation-of-ABHD5-protein-a-The.png)
ABHD5 protein structure and function. Schematic representation of ABHD5... | Download Scientific Diagram
![PDF) A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings PDF) A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings](https://i1.rgstatic.net/publication/338222320_A_novel_mutation_of_ABHD5_gene_in_a_Chanarin_Dorfman_patient_with_unusual_dermatological_findings/links/5fc3cdbf458515b79788b3b0/largepreview.png)
PDF) A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings
![Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/351f6092-9fb4-48d1-aac0-6372e6ff2792/ced14062-fig-0002-m.jpg)
Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library
![Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports](https://media.springernature.com/lw685/springer-static/image/art%3A10.1038%2Fs41598-021-04179-7/MediaObjects/41598_2021_4179_Fig2_HTML.png)
Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports
Scholarly Article or Book Chapter | Clinical and genetic characterization of Chanarin-Dorfman Syndrome patients: first report of large deletions in the ABHD5 gene | ID: m900nw69t | Carolina Digital Repository
![Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond - ScienceDirect Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1388198117301476-gr1.jpg)
Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond - ScienceDirect
Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome | European Journal of Translational Myology
![Molecular characterization of ABHD5 gene promoter in intramuscular preadipocytes of Qinchuan cattle: Roles of Evi1 and C/EBPα - ScienceDirect Molecular characterization of ABHD5 gene promoter in intramuscular preadipocytes of Qinchuan cattle: Roles of Evi1 and C/EBPα - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0378111918312873-gr5.jpg)