Study of Deafness Associated with DFNB59 Gene (pejvakin) Mutation in Fars Province
Background and Objectives: Hearing loss is the most frequent sensory disorder affecting 1 in 500 neonates with more than 50% of inherited cases. This trait is a very heterogeneous disorder and happens due to genetic or environmental causes or both. More than 46 genes may be involved in non-syndromic...
| Main Authors: | , , , , , , , , , |
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| Format: | Article |
| Language: | fas |
| Published: |
Qom University of Medical Sciences
2011-01-01
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| Series: | Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Qum |
| Subjects: | |
| Online Access: | http://journal.muq.ac.ir/library/upload/article/af_944563289.16.2.pdf |