WorldCat Identities

Kremer, Laura Sophie

Overview
Works: 5 works in 5 publications in 1 language and 38 library holdings
Roles: Author
Classifications: R1, 616.1
Publication Timeline
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Most widely held works by Laura Sophie Kremer
Discovery and validation of coding and non-coding pathogenic variants in mitochondrial disorders by Laura Sophie Kremer( )

1 edition published in 2017 in English and held by 31 WorldCat member libraries worldwide

"Transcriptomics": molecular diagnosis of inborn errors of metabolism via RNA-sequencing by Laura S Kremer( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

Bi-allelic mutations in NDUFA6 establish its role in early-onset isolated mitochondrial complex I deficiency by Charlotte Alston( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

Arabidopsis thaliana alternative dehydrogenases: a potential therapy for mitochondrial complex I deficiency? Perspectives and pitfalls by Alessia Catania( )

1 edition published in 2019 in English and held by 2 WorldCat member libraries worldwide

Genetic diagnosis of Mendelian disorders via RNA sequencing( )

1 edition published in 2017 in English and held by 1 WorldCat member library worldwide

 
Audience Level
0
Audience Level
1
  General Special  
Audience level: 0.00 (from 0.00 for Discovery ... to 0.00 for Discovery ...)

Alternative Names
Kremer, Laura Sophie

Languages