Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate-Reference-Cited by-同舟云学术

Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate

Published:2015-06-26 Issue:4 Volume:85 Page:306-315
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Anttonen Anna-Kaisa,Hilander Taru,Linnankivi Tarja,Isohanni Pirjo,French Rachel L.,Liu Yuchen,Simonović Miljan,Söll Dieter,Somer Mirja,Muth-Pawlak Dorota,Corthals Garry L.,Laari Anni,Ylikallio Emil,Lähde Marja,Valanne Leena,Lönnqvist Tuula,Pihko Helena,Paetau Anders,Lehesjoki Anna-Elina,Suomalainen Anu,Tyynismaa Henna

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference32 articles.

1. Infantile onset spinocerebellar ataxia with sensory neuropathy: A new inherited disease

2. Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky

3. Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation

4. Mitochondrial phenylalanyl-tRNA synthetase mutations underlie fatal infantile Alpers encephalopathy

5. Mechanisms of mitochondrial diseases

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