Associated Papers
De Novo Occurrence of a Variant in ARL3 and Apparent Autosomal Dominant Transmission of Retinitis Pigmentosa.
Strom SP et al.
Plos One, 2016
26964041 (PubMed )
Supplement: pone.0150944.s002.xls › All_variants
Rare variants in LRRK1 and Parkinson's disease.
Schulte EC et al.
Neurogenetics, 2014
24241507 (PubMed )
Supplement: 10048_2013_383_MOESM1_ESM.pdf
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