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Robuta

https://journal.muq.ac.ir/article-1-63-en.html
Study of Deafness Associated with DFNB59 Gene (pejvakin) Mutation in Fars Province - Qom University...
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...
studydeafnessassociatedgenepejvakin