Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease

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Genetic screening in two Iranian families with early-onset Alzheimer's disease identified a novel PSEN1 mutation.Parkinson disease: CSMD1 gene mutations can lead to familial Parkinson disease.

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Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease

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2017 nî lūn-bûn

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2017年学术文章

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Whole-exome sequencing associa ...... ith familial Parkinson disease

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Whole-exome sequencing associa ...... ith familial Parkinson disease

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Whole-exome sequencing associa ...... ith familial Parkinson disease

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Whole-exome sequencing associa ...... ith familial Parkinson disease

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Alberto Bergareche

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Javier Ruiz-Martínez

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Jose F Martí-Massó

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Luis J Azcona

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P2860

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Prediction of the coding sequences of unidentified human genes. XXI. The complete sequences of 60 new cDNA clones from brain which code for large proteins

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.

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e177

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scholarly article

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10.1212/NXG.0000000000000177

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P478

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Coro Paisán-Ruíz

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2017-08-02T00:00:00Z

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28808687

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Parkinson's disease

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5540655

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Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease

about

P2860

P2860

Whole-exome sequencing associates novel CSMD1 gene mutations with familial Parkinson disease

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P932