Search Results - "Takeichi, Norito"

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    The prevalence and clinical features of MYO7A-related hearing loss including DFNA11, DFNB2 and USH1B by Watanabe, Kizuki, Nishio, Shin-ya, Usami, Shin-ichi

    Published in Scientific reports (09-04-2024)
    “…The MYO7A gene is known to be responsible for both syndromic hearing loss (Usher syndrome type1B:USH1B) and non-syndromic hearing loss including autosomal…”
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    Journal Article