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Nonsyndromic 35 delG Mutation of the Connexin 26 Gene Associated With Deafness in Syndromic Children: Two Case Reports

✍ Scribed by Frédéric Venail; Anne-Françoise Roux; Nathalie Pallares-Ruiz; Mireille Claustres; Patricia Blanchet; Quentin Gardiner; Michel Mondain

No coin nor oath required. For personal study only.

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