Kateřina Hodaňová

1PUBLICATIONS
9CO-AUTHORS
Neurology and neuromuscular diseases
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Publications (1)

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|Apr 28, 2020
Spinal muscular atrophy caused by a novel Alu-mediated deletion of exons 2a-5 in SMN1 undetectable with routine genetic testing.

Ivana Jedličková, Anna Přistoupilová, Lenka Nosková

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Ivana Jedličková

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Anna Přistoupilová

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Lenka Nosková

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Filip Majer

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Viktor Stránecký

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Hana Hartmannová

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Helena Trešlová

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Peter Solár

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Stanislav Kmoch

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Ivana Jedličková

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Anna Přistoupilová

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Lenka Nosková

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Filip Majer

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