(Q50433062)
Statements
Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: a very mild phenotype. (English)
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Vincent Couloigner
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Françoise Denoyelle
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Laurence Jonard
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Sébastien Pierrot
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Malek Louha
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Souad Gherbi
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Sandrine Marlin
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23 August 2011
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55
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1
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56-58
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Identifiers
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