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Rare coding variants involving MYO7A and other genes encoding stereocilia link proteins in familial meniere disease
by
Roman-Naranjo, P.
,
Moleon, M.D.C.
,
Aran, I.
,
Escalera-Balsera, A.
,
Soto-Varela, A.
,
Bächinger, D.
,
Gomez-Fiñana, M.
,
Eckhard, A.H.
,
Lopez-Escamez, J.A.
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Hearing research
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Hearing Research
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Audiology & Speech-Language Pathology
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Genomics
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Hair Cells, Vestibular
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Hearing Loss
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Heterozygote
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Humans
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Inner Ear
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Life Sciences & Biomedicine
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Meniere Disease - Genetics
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Meniere's Disease
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Mutation
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Myosin Viia - Genetics
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Otorhinolaryngology
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Pedigree
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Elsevier:jisc Collections:elsevier Read And Publish Agreement 2022-2024:Freedom Collection (Reading List)
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