Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome | European Journal of Translational Myology
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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
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PDF) A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings
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PDF) A New Case of Chanarin-Dorfman Syndrome with a Novel Deletion in ABHD5 Gene | Hamed Heidary - Academia.edu
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ABHD5 protein structure and function. Schematic representation of ABHD5... | Download Scientific Diagram
![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
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Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
ABHD5 (abhydrolase domain containing 5, lysophosphatidic acid acyltransferase) | Gene Report | BioGPS
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Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports
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Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library
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The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
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