Hereditary hearing loss SNP-microarray pilot study

OBJECTIVES: Despite recent advancements in diagnostic tools, the genomic landscape of hereditary hearing loss remains largely uncharacterized. One strategy to understand genome-wide aberrations includes the analysis of copy number variation that can be mapped using SNP-microarray technology. A growi...

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Detalles Bibliográficos
Autores principales: Vona, Barbara, Hofrichter, Michaela A. H., Schröder, Jörg, Shehata-Dieler, Wafaa, Nanda, Indrajit, Haaf, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Data Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003021/
https://www.ncbi.nlm.nih.gov/pubmed/29903040
http://dx.doi.org/10.1186/s13104-018-3466-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003021/
https://www.ncbi.nlm.nih.gov/pubmed/29903040
http://dx.doi.org/10.1186/s13104-018-3466-7

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