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. [electronic resource]
Producer: 20061031Description: 752-8 p. digitalISSN:- 0002-9297
- Africa, Northern
- Amino Acid Substitution
- Case-Control Studies
- Family
- Female
- Haplotypes
- Humans
- Jews -- genetics
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Male
- Middle East
- Parkinson Disease -- genetics
- Polymorphism, Single Nucleotide
- Protein Serine-Threonine Kinases -- genetics
- Software
- White People -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
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