X‐chromosomal inactivation patterns in women with Fabry disease-Reference-Cited by-同舟云学术

X‐chromosomal inactivation patterns in women with Fabry disease

Published:2022-08-16 Issue:9 Volume:10 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Molec Gen & Gen Med

Author:

Wagenhäuser Laura¹,Rickert Vanessa¹,Sommer Claudia¹²,Wanner Christoph²³,Nordbeck Peter²⁴^ORCID,Rost Simone⁵,Üçeyler Nurcan¹²^ORCID

Affiliation:

1. Department of Neurology University of Würzburg Würzburg Germany

2. Fabry Centre for Interdisciplinary Therapy Würzburg (FAZIT) University of Würzburg Würzburg Germany

3. Department of Internal Medicine, Division of Nephrology University of Würzburg Würzburg Germany

4. Department of Internal Medicine, Division of Cardiology University of Würzburg Würzburg Germany

5. Institute of Human Genetics University of Würzburg Würzburg Germany

Funder

Deutsche Forschungsgemeinschaft

Takeda Pharmaceuticals International

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.2029

Reference32 articles.

1. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen‐receptor gene correlates with X chromosome inactivation;Allen R. C.;American Journal of Human Genetics,1992

2. Characterization of Classical and Nonclassical Fabry Disease: A Multicenter Study

3. Three New Loci for Determining X Chromosome Inactivation Patterns

4. Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age

5. Skewing of X-inactivation ratios in blood cells of aging women is confirmed by independent methodologies

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