Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

about

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

Item

http://www.wikidata.org/entity/Q49711797

description

2018 nî lūn-bûn

@nan

2018年の論文

@ja

2018年学术文章

@wuu

2018年学术文章

@zh

2018年学术文章

@zh-cn

2018年学术文章

@zh-hans

2018年学术文章

@zh-my

2018年学术文章

@zh-sg

2018年學術文章

@yue

2018年學術文章

@zh-hant

name

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@en

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@nl

type

Item

label

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@en

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@nl

prefLabel

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@en

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@nl

P1476

Mitochondrial DNA Deletions With Low-Level Heteroplasmy in Adult-Onset Myopathy.

@en

P2093

Andrew L Mammen

http://www.w3.org/2001/XMLSchema#string

Elizabeth Harlan Michelle

http://www.w3.org/2001/XMLSchema#string

Julie S Cohen

http://www.w3.org/2001/XMLSchema#string

Lisa Christopher-Stine

http://www.w3.org/2001/XMLSchema#string

Renkui Bai

http://www.w3.org/2001/XMLSchema#string

P2860

Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathy.

Mitochondrial complex I and III mutations and neutral-lipid storage in activated mononuclear macrophages and neutrophils: a case presenting with necrotizing myopathy, poikiloderma atrophicans vasculare, and xanthogranulomatous bursitis.

Necrotizing myopathies: beyond statins.

SLC25A4 and C10ORF2 Mutations in Autosomal Dominant Progressive External Ophthalmoplegia.

Mitochondrial DNA-deletion mutations accumulate intracellularly to detrimental levels in aged human skeletal muscle fibers.

Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease.

Diagnosis and treatment of mitochondrial myopathies

Diagnostic challenges of mitochondrial DNA disorders.

Mitochondrial DNA genetics and the heteroplasmy conundrum in evolution and disease.

Disease progression in patients with single, large-scale mitochondrial DNA deletions.

P304

117-123

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1097/CND.0000000000000200

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Doris G. Leung

P577

2018-03-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29465611

http://www.w3.org/2001/XMLSchema#string

P921

mitochondrial DNA

P932

5824425

http://www.w3.org/2001/XMLSchema#string