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Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation inEXOSC3

✍ Scribed by Zanni, Ginevra; Scotton, Chiara; Passarelli, Chiara; Fang, Mingyan; Barresi, Sabina; Dallapiccola, Bruno; Wu, Bin; Gualandi, Francesca; Ferlini, Alessandra; Bertini, E.; Wei, Wang

Book ID: 121079495
Publisher: Springer
Year: 2013
Tongue: English
Weight: 275 KB
Volume: 14
Category: Article
ISSN: 1364-6745
DOI: 10.1007/s10048-013-0371-z

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