A number sign (#) is used with this entry because of evidence that Kufor-Rakeb syndrome (KRS), also known as Parkinson disease-9 (PARK9), is caused by homozygous or compound heterozygous mutation in the ATP13A2 gene (610513), which encodes a lysosomal type 5 ATPase, on chromosome 1p36. Description. Kufor-Rakeb syndrome is a rare autosomal ...
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