Autosomal dominant mitochondrial membrane protein‐associated neurodegeneration (MPAN)-Reference-Cited by-同舟云学术

Autosomal dominant mitochondrial membrane protein‐associated neurodegeneration (MPAN)

Published:2019-05-13 Issue:7 Volume:7 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Gregory Allison¹^ORCID,Lotia Mitesh²,Jeong Suh Young¹^ORCID,Fox Rachel¹,Zhen Dolly¹,Sanford Lynn¹,Hamada Jeff¹,Jahic Amir³^ORCID,Beetz Christian³,Freed Alison¹,Kurian Manju A.⁴,Cullup Thomas⁵,Weijden Marlous C. M.⁶,Nguyen Vy⁷,Setthavongsack Naly⁷,Garcia Daphne⁷,Krajbich Victoria⁷,Pham Thao⁷,Woltjer Randy⁷,George Benjamin P.⁸,Minks Kelly Q.⁸,Paciorkowski Alexander R.⁸⁹,Hogarth Penelope¹,Jankovic Joseph²,Hayflick Susan J.¹^ORCID

Affiliation:

1. Molecular & Medical Genetics, Pediatrics and Neurology Oregon Health & Science University Portland Oregon

2. Parkinson's Disease Center and Movement Disorder Clinic, Department of Neurology Baylor College of Medicine Houston Texas

3. Department of Clinical Chemistry Jena University Hospital Jena Germany

4. Developmental Neurosciences, GOSH‐Institute of Child Health, UCL & Department of Neurology Great Ormond Street Hospital London UK

5. North East Thames Regional Genetics Laboratory London UK

6. Department of Neurology University Medical Center Groningen Groningen The Netherlands

7. Pathology Oregon Health & Science University Portland Oregon

8. Department of Neurology University of Rochester Medical Center Rochester New York

9. Departments of Pediatrics, Biomedical Genetics, and Neuroscience University of Rochester Medical Center Rochester New York

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.736

Reference13 articles.

1. High frequency of partial SPAST deletions in autosomal dominant hereditary spastic paraplegia

2. Dominant versus recessive traits conveyed by allelic mutations - to what extent is nonsense-mediated decay involved?

3. Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

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