Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3.
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| Description | scientific article published on 24 August 2013 |
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author: Bruno Dallapiccola Chiara Passarelli Sabina Barresi Chiara Scotton Alessandra Ferlini Mingyan Fang Francesca Gualandi Ginevra Zanni Enrico Bertini |
| Publication date | August 24, 2013 |
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