Efficient detection of alport syndromeCOL4a5 mutations with multiplex genomic PCR-SSCP
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference54 articles.
1. HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS
2. Identification of Mutations in the COL4A5 Collagen Gene in Alport Syndrome
3. Definition and mapping of STSs at STR and RFLP loci in Xp11-Xq22
4. Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q
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3. Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay;Molecular Genetics & Genomic Medicine;2020-06-16
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