Preliminary observations of mitochondrial dysfunction in Prader-Willi syndrome-Reference-Cited by-同舟云学术

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Preliminary observations of mitochondrial dysfunction in Prader-Willi syndrome

Published:2018-10-05 Issue:12 Volume:176 Page:2587-2594
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Butler Merlin G.¹^ORCID,Hossain Waheeda A.¹,Tessman Robert²,Krishnamurthy Partha C.²

Affiliation:

1. Departments of Psychiatry & Behavioral Sciences and Pediatrics; University of Kansas Medical Center; Kansas City Kansas

2. Department of Pharmacology, Toxicology, & Therapeutics; University of Kansas Medical Center; Kansas City Kansas

Funder

National Center for Research Resources

National Institute of Environmental Health Sciences

National Institute of General Medical Sciences

Prayer-Will support and Kyleigh Ellington Family

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40526/fullpdf

Reference39 articles.

1. Top-down control analysis of systems with more than one common intermediate;Ainscow;European Journal of Biochemistry,1995

2. Energy metabolism profile in individuals with Prader-Willi syndrome and implications for clinical management: A systematic review;Alsaif;Advances in Nutrition,2017

3. Prader-Willi syndrome: A review of clinical, genetic, and endocrine findings;Angulo;Journal of Endocrinological Investigation,2015

4. Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations;Ashley;Human Molecular Genetics,2008

5. Microarray analysis of gene/transcript expression in Prader-Willi syndrome: Deletion versus UPD;Bittel;Journal of Medical Genetics,2003

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