Complement C4 Gene Copy Number Variation Genotyping by High Resolution Melting PCR
Background: Complement C4 gene copy number variation plays an important role as a determinant of genetic susceptibility to common diseases, such as systemic lupus erythematosus, schizophrenia, rheumatoid arthritis, and infectious diseases. This study aimed to develop an assay for the quantification...
Main Authors: | Claudia P. Jaimes-Bernal, Monte Trujillo, Francisco José Márquez, Antonio Caruz |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-08-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/21/17/6309 |
Similar Items
-
Genome-wide copy number variations in Bhutia equine breed using SNP genotyping data
by: NITESH KUMAR SHARMA, et al.
Published: (2023-08-01) -
A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples
by: Xiya Zhou, et al.
Published: (2021-01-01) -
A Potential Method to Help Predict Genetic Diseases and Arrange Healthcare: Copy Number Variation Analysis
by: Munis Dündar, et al.
Published: (2019-11-01) -
Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia
by: Xing Xin, et al.
Published: (2023-09-01) -
Genome-wide copy number variation detection in a large cohort of diverse horse breeds by whole-genome sequencing
by: Xiangwei Tang, et al.
Published: (2023-11-01)