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]
- American journal of human genetics Oct 2006
- 752-8 p. digital
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.
0002-9297
10.1086/508025 doi
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