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Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild

Laurence Jonard1, Vincent Couloigner, Sébastien Pierrot

  • 1Centre de référence des surdités génétiques, Trousseau Hospital, Paris, France.

European Journal of Medical Genetics
|September 6, 2011
PubMed

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