Service interruption on Monday 11 July from 12:30 to 13:00: all the sites of the CCSD (HAL, Epiciences, SciencesConf, AureHAL) will be inaccessible (network hardware connection).
Skip to Main content Skip to Navigation
Journal articles

Whole exome sequencing may be insufficient to cover the causality spectrum of rhabdomyolysis

Josef Finsterer 1, * Sinda Zarrouk-Mahjoub 2 
* Corresponding author
1 Krankenanstalt Rudolfstiftung
2 LR11IPT05 - Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory
Abstract : Correspondance
Keywords : Genotype Mitochondrial Pathogenicity Phenotype Rhabdomyolysis Whole exome sequencing mtDNA
Document type :
Journal articles
Complete list of metadata

Cited literature [3 references]  Display  Hide  Download
https://hal-riip.archives-ouvertes.fr/pasteur-02003296
Contributor : AbdelHakim Ben Hassine Connect in order to contact the contributor
Submitted on : Friday, February 1, 2019 - 11:26:36 AM
Last modification on : Wednesday, October 28, 2020 - 9:52:05 AM

File

Vignette du document
Whole exome.pdf
Publication funded by an institution

Licence

Distributed under a Creative Commons Attribution 4.0 International License

Identifiers

Collections

RIIP | RIIP_TUNIS

Citation

Josef Finsterer, Sinda Zarrouk-Mahjoub. Whole exome sequencing may be insufficient to cover the causality spectrum of rhabdomyolysis. Molecular Genetics and Metabolism Reports, Elsevier, 2018, 17, pp.18. ⟨10.1016/j.ymgmr.2018.08.001⟩. ⟨pasteur-02003296⟩

Export

BibTeX TEI DC DCterms EndNote Datacite

Share

Metrics

Record views

10

Files downloads

53