(Q28257086)

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Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

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title

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease (English)

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1 reference

3

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Daniela Berg

series ordinal

6

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ORCID Public Data File 2021

Rejko Krüger

series ordinal

15

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Hartwig Wolburg

series ordinal

11

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Julian Downward

series ordinal

12

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Jörg B. Schulz

object named as

Jörg B Schulz

series ordinal

14

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Thomas Gasser

series ordinal

7

object named as

Thomas Gasser

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Olaf Riess

series ordinal

13

object named as

Olaf Riess

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author name string

Karsten M Strauss

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1

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L Miguel Martins

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2

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Frank P Marx

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4

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Sabine Kautzmann

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5

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Zbginiew Wszolek

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8

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Thomas Müller

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9

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Antje Bornemann

series ordinal

10

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language of work or name

English

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publication date

1 August 2005

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published in

Human Molecular Genetics

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volume

14

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page(s)

2099-111

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issue

15

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cites work

Binding specificity and regulation of the serine protease and PDZ domains of HtrA2/Omi

1 reference

2 April 2022

https://opencitations.net/index/coci/api/v1/citations/10.1074/JBC.M308659200

GENEPOP (Version 1.2): Population Genetics Software for Exact Tests and Ecumenicism

1 reference

20 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1093/OXFORDJOURNALS.JHERED.A111573

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/33416

Identifiers

DOI

10.1093/HMG/DDI215

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Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5582

OpenCitations bibliographic resource ID

5582

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

5582

(Q28257086)

Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease

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