Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome (Q85851515)

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scientific article published on 16 August 2013
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Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome
scientific article published on 16 August 2013

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    Homozygosity for a novel truncating mutation confirms TBX15 deficiency as the cause of Cousin syndrome (English)

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