Funder
U.S. Department of Health & Human Services | NIH | National Institute on Deafness and Other Communication Disorders
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference33 articles.
1. Corvino V, Apisa P, Malesci R, Laria C, Auletta G, Franze A. X-linked sensorineural hearing loss: a literature review. Curr Genomics. 2018;19:327–38.
2. Knebelmann B, Breillat C, Forestier L, Arrondel C, Jacassier D, Giatras I, et al. Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome. Am J Hum Genet. 1996;59:1221.
3. Plant KE, Green PM, Vetrie D, Flinter FA. Detection of mutations in COL4A5 in patients with Alport syndrome. Hum Mutat. 1999;13:124–32.
4. Wang F, Ding J, Yu Lx, Yang Jy. Detection of COL4A5 gene mutations in Alport syndrome by analyzing cDNA of skin fibroblasts. J Beijing Med Univ. 2002;3:219–224.
5. Mothes H, Heidet L, Arrondel C, Richter KK, Thiele M, Patzer L, et al. Alport syndrome associated with diffuse leiomyomatosis: COL4A5‐COL4A6 deletion associated with a mild form of Alport nephropathy. Nephrol Dial Transplant. 2002;17:70–4.
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