Huntington Disease: Molecular Diagnostics Approach-Reference-Cited by-同舟云学术

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Huntington Disease: Molecular Diagnostics Approach

Published:2015-10 Issue:1 Volume:87 Page:
ISSN:1934-8266
Container-title:Current Protocols in Human Genetics
language:en
Short-container-title:Current Protocols in Human Genetics

Author:

Bastepe Murat¹²³,Xin Winnie¹⁴

Affiliation:

1. Neurogenetics DNA Diagnostic Laboratory, Department of Neurology, Massachusetts General Hospital and Harvard Medical School Boston Massachusetts

2. Genetics Training Program, Harvard Medical School Boston Massachusetts

3. Endocrine Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School Boston Massachusetts

4. Center for Human Genetic Research, Massachusetts General Hospital and Harvard Medical School Boston Massachusetts

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/0471142905.hg0926s87

Reference26 articles.

1. A CCG repeat polymorphism adjacent to the CAG repeat in the Huntington disease gene: implications for diagnostic accuracy and predictive testing

2. American College of Medical Genetics and Genomics Standards and Guidelines for Clinical Genetics Laboratories, 2014 edition: technical standards and guidelines for Huntington disease

3. Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas

4. A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease

5. Southern transfer protocol for confirmation of Huntington disease;Guida M.;Clin. Chem.,1996

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1. Huntingtin CAG repeat size variations outside the Huntington’s disease complex: associations with depression and anxiety phenotypes and basal ganglia structure;2024-05-22

2. Métodos diagnósticos moleculares en enfermedades neuromusculares y neurodegenerativas de origen genético;Pediatría;2024-03-30

3. Environmental and genetic risk factors for Parkinson’s disease;Bulletin of Siberian Medicine;2023-01-21

4. ATTCT and ATTCC repeat expansions in the ATXN10 gene affect disease penetrance of spinocerebellar ataxia type 10;Human Genetics and Genomics Advances;2022-10

5. Molecular Diagnostics and Immunological Markers of Neurodegenerative Disorders;Neurodegenerative Diseases: Multifactorial Degenerative Processes, Biomarkers and Therapeutic Approaches (First Edition);2022-08-09

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