Role of myelin basic protein and proteolipid protein genes in multiple sclerosis: single strand conformation polymorphism analysis of the human sequences-Reference-Cited by-同舟云学术

Role of myelin basic protein and proteolipid protein genes in multiple sclerosis: single strand conformation polymorphism analysis of the human sequences

Published:1997-12 Issue:6 Volume:23 Page:457-467
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathology and Applied Neurobiology

Author:

Price S. E.¹,Sharpe G.¹,Boots A.¹,Poutsma A.¹,Mason C.¹,James J.¹,Hinks L.¹,Thompson R. J.¹

Affiliation:

1. Wessex Human Genetics Institute, Southampton General Hospital, Southampton, UK

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-2990.1997.tb01322.x

Reference42 articles.

1. DNA length polymorphism 5? to the myelin basic protein gene is associated with multiple sclerosis

2. Repetitive DNA (TGGA)n 5′ to the human myelin basic protein gene: A new form of oligonucleotide repetitive sequence showing length polymorphism

3. IDENTITY OF MYELIN BASIC PROTEIN FROM MULTIPLE SCLEROSIS AND HUMAN CONTROL BRAINS: DISCOVERY OF A GENETIC VARIANT

4. Individual exons encode the integral membrane domains of human myelin proteolipid protein.

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