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SNP information rs11564148

RS11564148

Normal allele: TT

Low levels of LRRK2 gene expression contribute to the progression of Parkinson's disease.

Polymorphism rs11564148 is related to topics like this:

Parkinson is a genetic disease

A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...

Research and publications:

  15726496   Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations.

  16960813   LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

  18952485   Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.

  19343804   LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.

  20301387   LRRK2 Parkinson Disease.

  20669299   LRRK2 variation and Parkinson's disease in African Americans.

  21885347   Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.

  29376065   Haplotype-Contained PCR Products Analysis by Sequencing with Selective Restriction of Primer Extension.

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Dementia is genetic

Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...

Alzheimer's disease is hereditary

Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...

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