A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome (Q34277615)
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English | A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome |
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A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome (English)
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Tally Lerman-Sagie
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Dorit Lev
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Lubov Blumkin
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Sara Kivity
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Sarit Cohen
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Ruth Shomrat
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26 May 2012
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259
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12
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2590-2598
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