Slc22a5 haploinsufficiency does not aggravate the phenotype of the long‐chain acyl‐CoA dehydrogenase KO mouse-Reference-Cited by-同舟云学术

Slc22a5 haploinsufficiency does not aggravate the phenotype of the long‐chain acyl‐CoA dehydrogenase KO mouse

Published:2019-12-23 Issue:3 Volume:43 Page:486-495
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:Jrnl of Inher Metab Disea

Author:

Ranea‐Robles Pablo¹^ORCID,Yu Chunli¹²,Vlies Naomi³⁴,Vaz Frédéric M.⁴,Houten Sander M.¹^ORCID

Affiliation:

1. Department of Genetics and Genomic Sciences Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai New York New York

2. Mount Sinai Genomics, Inc. New York New York

3. Institute for Translational Vaccinology Bilthoven The Netherlands

4. Department of Clinical Chemistry, Amsterdam Gastroenterology & Metabolism Laboratory Genetic Metabolic Diseases, Amsterdam UMC, University of Amsterdam Amsterdam The Netherlands

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12204

Reference33 articles.

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3. Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood