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Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3 |
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Titel: |
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3 |
Auteur: |
Zanni, Ginevra Scotton, Chiara Passarelli, Chiara Fang, Mingyan Barresi, Sabina Dallapiccola, Bruno Wu, Bin Gualandi, Francesca Ferlini, Alessandra Bertini, E. Wei, Wang |
Verschenen in: |
Neurogenetics |
Paginering: |
Jaargang 14 (2013) nr. 3-4 pagina's 247-250 |
Jaar: |
2013 |
Inhoud: |
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Uitgever: |
Springer Berlin Heidelberg, Berlin/Heidelberg |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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