التفاصيل البيبلوغرافية
| العنوان: |
Diagnostic pitfalls for GJB2‐related hearing loss: A novel deletion detected by Array‐CGH analysis in a Japanese patient with congenital profound hearing loss. |
| المؤلفون: |
Abe, Satoko, Nishio, Shin‐ya, Yokota, Yoh, Moteki, Hideaki, Kumakawa, Kozo, Usami, Shin‐ichi |
| المصدر: |
Clinical Case Reports; Nov2018, Vol. 6 Issue 11, p2111-2116, 6p |
| مصطلحات موضوعية: |
DNA copy number variations, GENE expression, HEARING disorders, CHROMOSOME abnormalities |
| مستخلص: |
Key Clinical Message: Here, we report a novel deletion (copy number variation: CNV) in the GJB2 gene observed in a Japanese hearing loss patient. The deleted segment started in the middle of the GJB2 gene, but the GJB6 gene remained intact. This partial deletion in the GJB2 gene highlights the need for further improvements in GJB2 screening. Here, we report a novel deletion in the GJB2 gene observed in a Japanese hearing loss patient. The deleted segment started in the middle of the GJB2 gene, but the GJB6 gene remained intact. This partial deletion in the GJB2 gene highlights the need for further improvements in GJB2 screening. [ABSTRACT FROM AUTHOR] |
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| قاعدة البيانات: |
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