Related Articles
A novel missense mutation in <em>SPAST</em> causes hereditary spastic paraplegia in male members of a family: A case report
Novel compound heterozygous PKHD1 mutations cause autosomal recessive polycystic kidney disease in a Han Chinese family
A novel frameshift mutation in the <em>FERMT1</em> gene in a Chinese patient with Kindler syndrome
A novel <em>KCNQ4</em> gene variant (c.857A>G; p.Tyr286Cys) in an extended family with non‑syndromic deafness 2A
Identification of a novel pathogenic <em>COL4A3</em> gene mutation in a Chinese family with autosomal dominant Alport syndrome: A case report