Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients ; volume:04 ; number:04 ; year:2020 ; pages:e322-e331
TH open ; 04, Heft 04 (2020), e322-e331

Contributor: Manderstedt, Eric
Lind-Halldén, Christina
Lethagen, Stefan
Halldén, Christer

DOI: 10.1055/s-0040-1718885

URN: urn:nbn:de:101:1-2021012008515077448149

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:33 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Manderstedt, Eric
Lind-Halldén, Christina
Lethagen, Stefan
Halldén, Christer

Other Objects (12)

Two Variants of Canine von Willebrand’s Disease

Reduced Antigenic Reactivity in “Variants” of von Willebrand’s Disease

Prothrombotic Variants of von Willebrand Factor (VWF)

Hochschulschrift

Association analysis of rare genomic variants

Aufsatzsammlung

Analyzing rare variants in complex diseases

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

New rare genetic variants in multiple sclerosis

Rare variants in LRRK1 and Parkinson's disease

Bestand

Willebrand (Bestand)

Archivale

Willebrand, Alfons

Archivale

Busch, Willebrand

Archivale

Willebrand, Bernhard

Two Variants of Canine von Willebrand’s Disease

Reduced Antigenic Reactivity in “Variants” of von Willebrand’s Disease

Prothrombotic Variants of von Willebrand Factor (VWF)

Hochschulschrift

Association analysis of rare genomic variants

Aufsatzsammlung

Analyzing rare variants in complex diseases

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

New rare genetic variants in multiple sclerosis

Rare variants in LRRK1 and Parkinson's disease

Bestand

Willebrand (Bestand)

Archivale

Willebrand, Alfons

Archivale

Busch, Willebrand

Archivale

Willebrand, Bernhard

Two Variants of Canine von Willebrand’s Disease

Reduced Antigenic Reactivity in “Variants” of von Willebrand’s Disease

Prothrombotic Variants of von Willebrand Factor (VWF)

Hochschulschrift

Association analysis of rare genomic variants

Aufsatzsammlung

Analyzing rare variants in complex diseases

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

New rare genetic variants in multiple sclerosis

Rare variants in LRRK1 and Parkinson's disease

Bestand

Willebrand (Bestand)

Archivale

Willebrand, Alfons

Archivale

Busch, Willebrand

Archivale

Willebrand, Bernhard

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Two Variants of Canine von Willebrand’s Disease

Reduced Antigenic Reactivity in “Variants” of von Willebrand’s Disease

Prothrombotic Variants of von Willebrand Factor (VWF)

Association analysis of rare genomic variants

Analyzing rare variants in complex diseases

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

New rare genetic variants in multiple sclerosis

Rare variants in LRRK1 and Parkinson's disease

Willebrand (Bestand)

Willebrand, Alfons

Busch, Willebrand

Willebrand, Bernhard

Two Variants of Canine von Willebrand’s Disease

Reduced Antigenic Reactivity in “Variants” of von Willebrand’s Disease

Prothrombotic Variants of von Willebrand Factor (VWF)

Association analysis of rare genomic variants

Analyzing rare variants in complex diseases

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

New rare genetic variants in multiple sclerosis

Rare variants in LRRK1 and Parkinson's disease

Willebrand (Bestand)

Willebrand, Alfons

Busch, Willebrand

Willebrand, Bernhard

Two Variants of Canine von Willebrand’s Disease

Reduced Antigenic Reactivity in “Variants” of von Willebrand’s Disease

Prothrombotic Variants of von Willebrand Factor (VWF)

Association analysis of rare genomic variants

Analyzing rare variants in complex diseases

Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients

New rare genetic variants in multiple sclerosis

Rare variants in LRRK1 and Parkinson's disease

Willebrand (Bestand)

Willebrand, Alfons

Busch, Willebrand

Willebrand, Bernhard

Related objects

Reset password