(Q34157065)
Statements
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Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I. (English)
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Mary M Reilly
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Christian Guelly
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Peng-Peng Zhu
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Lea Leonardis
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Lea Papić
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Janez Zidar
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Maria Schabhüttl
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Heimo Strohmaier
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Joachim Weis
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Tim M Strom
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Jonathan Baets
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Jan Willems
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Peter De Jonghe
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Martina Hatz
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Slave Trajanoski
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Thomas R Pieber
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Craig Blackstone
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30 December 2010
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88
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99-105
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Identifiers
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