An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome (Q34980853)
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English | An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome |
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An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome (English)
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Kerstin Kutsche
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Hengameh Abdollahpour
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Malik Alawi
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Fanny Kortüm
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Michael Beckstette
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Eva Seemanova
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Vladimír Komárek
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Georg Rosenberger
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30 April 2014
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