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Dokumenttyp:
Journal Article; Research Support, Non-U.S. Gov't
Autor(en):
Haack, TB; Haberberger, B; Frisch, EM; Wieland, T; Iuso, A; Gorza, M; Strecker, V; Graf, E; Mayr, JA; Herberg, U; Hennermann, JB; Klopstock, T; Kuhn, KA; Ahting, U; Sperl, W; Wilichowski, E; Hoffmann, GF; Tesarova, M; Hansikova, H; Zeman, J; Plecko, B; Zeviani, M; Wittig, I; Strom, TM; Schuelke, M; Freisinger, P; Meitinger, T; Prokisch, H
Titel:
Molecular diagnosis in mitochondrial complex I deficiency using exome sequencing.
Abstract:
Next generation sequencing has become the core technology for gene discovery in rare inherited disorders. However, the interpretation of the numerous sequence variants identified remains challenging. We assessed the application of exome sequencing for diagnostics in complex I deficiency, a disease with vast genetic heterogeneity.Ten unrelated individuals with complex I deficiency were selected for exome sequencing and sequential bioinformatic filtering. Cellular rescue experiments were performed...     »
Zeitschriftentitel:
J Med Genet
Jahr:
2012
Band / Volume:
49
Heft / Issue:
4
Seitenangaben Beitrag:
277-83
Sprache:
eng
Volltext / DOI:
doi:10.1136/jmedgenet-2012-100846
PubMed:
http://view.ncbi.nlm.nih.gov/pubmed/22499348
Print-ISSN:
0022-2593
TUM Einrichtung:
Institut für Humangenetik; Institut für Medizinische Statistik und Epidemiologie
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