PDF) A New Case of Chanarin-Dorfman Syndrome with a Novel Deletion in ABHD5 Gene | Hamed Heidary - Academia.edu
Abhd5 Gene Expression Results - GXD
ABHD5 - Wikipedia
Recurrent N209* ABHD5 mutation in two unreported families with Chanarin Dorfman Syndrome | European Journal of Translational Myology
ABHD5 cleaves HDAC4 to benefit the heart | Nature Metabolism
A) Sequence analysis of ABHD5 gene in the proband and her sister.... | Download Scientific Diagram
Gene: ABHD5 (ENSG00000011198) - Summary - Homo_sapiens - Ensembl genome browser 109
Molecular analysis of Chanarin-Dorfman syndrome (CDS) patients: Identification of novel mutations in the ABHD5 gene. | Semantic Scholar
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
Metabolites | Free Full-Text | ABHD5—A Regulator of Lipid Metabolism Essential for Diverse Cellular Functions
Chanarin–Dorfman syndrome: a novel homozygous mutation in the ABHD5 gene - Al‐Hage - 2020 - Clinical and Experimental Dermatology - Wiley Online Library
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
A New Patient of Chanarin Dorfman Syndrome in Egypt
Frontiers | Recent Advances on the Role of ATGL in Cancer
What is ABHD5 Gene Chanarin-Dorfman syndrome NGS Genetic DNA Test ?
ABHD5 (abhydrolase domain containing 5, lysophosphatidic acid acyltransferase) | Gene Report | BioGPS
A novel mutation of ABHD5 gene in a Chanarin Dorfman patient with unusual dermatological findings | Lipids in Health and Disease | Full Text
ABHD5 Antibody (E-1) | SCBT - Santa Cruz Biotechnology
ABHD5 (h): 293 Lysate: sc-112234
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Structural and functional insights into ABHD5, a ligand-regulated lipase co-activator | Scientific Reports
The lipid-droplet-associated protein ABHD5 protects the heart through proteolysis of HDAC4 | Nature Metabolism
ABHD5 Gene - GeneCards | ABHD5 Protein | ABHD5 Antibody
Schematic model of ABHD5 domain structure. The blue area marks the... | Download Scientific Diagram
Fat breakdown: A function for CGI-58 (ABHD5) provides a new piece of the puzzle: Cell Metabolism
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
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
