Associated Papers
Mutations in MT-ATP6 are a frequent cause of adult-onset spinocerebellar ataxia.
Nolte D et al.
Journal of Neurology, 2021
Targeted resequencing identifies PTCH1 as a major contributor to ocular developmental anomalies and extends the SOX2 regulatory network.
Chassaing N et al.
Genome Research, 2016
26893459 (PubMed )
Supplement: supp_gr.196048.115_Supp_Tables_2-7.docx
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