Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3

G Zanni, C Scotton, C Passarelli, M Fang, S Barresi… - Neurogenetics, 2013 - Springer
Whole exome sequencing in two-generational kindred from Bangladesh with early onset
spasticity, mild intellectual disability, distal amyotrophy, and cerebellar atrophy transmitted …
被引用次数：47 相关文章

Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3

G Zanni, C Scotton, C Passarelli, M Fang… - …, 2013 - search.proquest.com
Whole exome sequencing in two-generational kindred from Bangladesh with early onset
spasticity, mild intellectual disability, distal amyotrophy, and cerebellar atrophy transmitted …

Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3.

G Zanni, C Scotton, C Passarelli, M Fang, S Barresi… - Neurogenetics, 2013 - europepmc.org
Whole exome sequencing in two-generational kindred from Bangladesh with early onset
spasticity, mild intellectual disability, distal amyotrophy, and cerebellar atrophy transmitted …

[引用][C] Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3

G Zanni, C Scotton, C Passarelli, M Fang, S Barresi… - neurogenetics, 2013 - cir.nii.ac.jp
Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar
atrophy detects a novel mutation in EXOSC3 | CiNii Research CiNii 国立情報学研究所 学術 …

Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3

G Zanni, C Scotton, C Passarelli, M Fang, S Barresi… - neurogenetics, 2013 - infona.pl
Whole exome sequencing in two-generational kindred from Bangladesh with early onset
spasticity, mild intellectual disability, distal amyotrophy, and cerebellar atrophy transmitted …

Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3

G Zanni, C Scotton, C Passarelli, M Fang… - …, 2013 - pubmed.ncbi.nlm.nih.gov
Whole exome sequencing in two-generational kindred from Bangladesh with early onset
spasticity, mild intellectual disability, distal amyotrophy, and cerebellar atrophy transmitted …

[引用][C] Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3

G Zanni, C Scotton, C Passarelli, M Fang, S Barresi… - Neurogenetics, 2013 - Springer