A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.
about
Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.Splicing: is there an alternative contribution to Parkinson's disease?Leucine-Rich Repeat Kinase (LRRK2) Genetics and Parkinson's Disease.The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from southern Italy.PRKN, DJ-1, and PINK1 screening identifies novel splice site mutation in PRKN and two novel DJ-1 mutations.
P2860
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年学术文章
@wuu
2009年学术文章
@zh-cn
2009年学术文章
@zh-hans
2009年学术文章
@zh-my
2009年学术文章
@zh-sg
2009年學術文章
@yue
2009年學術文章
@zh
2009年學術文章
@zh-hant
name
A clinic-based screening of mu ...... Parkinson's disease patients.
@en
A clinic-based screening of mu ...... Parkinson's disease patients.
@nl
type
label
A clinic-based screening of mu ...... Parkinson's disease patients.
@en
A clinic-based screening of mu ...... Parkinson's disease patients.
@nl
altLabel
A clinic-based screening of mu ...... n Parkinson's disease patients
@en
prefLabel
A clinic-based screening of mu ...... Parkinson's disease patients.
@en
A clinic-based screening of mu ...... Parkinson's disease patients.
@nl
P2093
P2860
P356
P1433
P1476
A clinic-based screening of mu ...... n Parkinson's disease patients
@en
P2093
Elahe Elahi
Farzad Sina
Farzaneh Ghazavi
Gholam-Ali Shahidi
Homa Sadeghi
Khosro Parsa
Mostafa Ronaghi
Niloofar Farboodi
Seyedmehdi Shojaee
Zeinab Fazlali
P2860
P304
P356
10.1002/MDS.22503
P4011
96497e69c18c72c2194f11e590eaa85a55b36879
P407
P577
2009-05-01T00:00:00Z