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Characterization of copy number variants (CNVs) identified by genetic testing of inherited retinal disorders
Characterization of copy number variants (CNVs) identified by genetic testing of inherited retinal disorders
2019
Lucia Guidugli
Miika Mehine
Sari Tuupanen
Kati Kämpjärvi
Kirsty Wells
Johanna Känsäkoski
Miko Valori
Inka Saarinen
Mikko Muona
Eeva-Marja Sankila
Samuel Myllykangas
Juha Koskenvuo
Tero-Pekka Alastalo
Keywords:
Genetic testing
Retinal Disorder
Biology
Genetics
Copy-number variation
Correction
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