Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls
- Auteur
- SIMON-SANCHEZ, Javier1 2 ; SINGLETON, Andrew B1 3
[1] Molecular Genetics Unit, Laboratory of Neurogenetics, National Institute on Aging, National Institutes of Health, Bethesda, MD 20892, United States
[2] Unidad de Genética Molecular, Departamento de Genómica y Proteómica, Instituto de Biomedicina de Valencia-CSIC, 46010, Valencia, Spain
[3] Department of Public Health Sciences, Center for Public Health Genomics, University of Virginia, Charlottesville, VA 22908, United States - Source
Human molecular genetics (Print). 2008, Vol 17, Num 13, pp 1988-1993, 6 p ; ref : 26 ref
- Editeur
- Oxford University Press, Oxford
- Pays de publication
- United Kingdom
- Type de document
- Article
- Langue
- English
- Mot clé (fr)
- Génétique Mutation Normal Pathogène Régulation Séquençage
- Mot clé (en)
- Genetics Mutation Normal Pathogenic Regulation(control) Sequencing
- Mot clé (es)
- Genética Mutación Normal Patógeno Regulación Sequencing
- Classification
- Pascal
- 002 Sciences biologiques et medicales / 002A Sciences biologiques fondamentales et appliquees. Psychologie / 002A04 Biologie moleculaire et cellulaire
- Pascal
- 002 Sciences biologiques et medicales / 002A Sciences biologiques fondamentales et appliquees. Psychologie / 002A07 Genetique des eucaryotes. Evolution biologique et moleculaire
- Discipline
- Eukaryotes genetics. Biological and molecular evolution Molecular and cell biology
- Provenance
- Inist-CNRS
- Base de données
- PASCAL
- Identifiant INIST
- 20433933
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1093/hmg/ddn096 
https://dx.doi.org/10.1093/hmg/ddn096
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