about
Identification of a novel collagen type IV alpha-4 (COL4A4) mutation in a Chinese family with autosomal dominant Alport syndrome using exome sequencing.Alport syndrome: facts and opinions.The Variability of Estimated Glomerular Filtration Rate Decline in Alport Syndrome.Genomic medicine for kidney disease.Functional assessment of a novel COL4A5 splice region variant and immunostaining of plucked hair follicles as an alternative method of diagnosis in X-linked Alport syndrome.Temporal retinal thinning and the diagnosis of Alport syndrome and Thin basement membrane nephropathy.Alport syndrome and Pierson syndrome: Diseases of the glomerular basement membrane.
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Q37550885-26C1521F-B9B4-4FBC-BE49-D7B3BB565B30Q37595448-B5A1449A-1205-4557-9D88-EB962E953971Q41070836-E9014C1E-797C-4056-88FC-A0AEC339A54CQ47200436-D0D476BD-B674-4469-8082-25673481811EQ47908601-4EF0024A-C2E4-41C0-A1E8-E495668B4159Q49666677-43A3799C-2F53-448B-87A2-83AA11B20513Q52718217-D51DAFA0-5DE8-4C1C-A4D6-E08D52C63466
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description
2016 nî lūn-bûn
@nan
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
2016年论文
@zh
2016年论文
@zh-cn
name
Alport Syndrome in Women and Girls.
@en
type
label
Alport Syndrome in Women and Girls.
@en
prefLabel
Alport Syndrome in Women and Girls.
@en
P2093
P2860
P356
P1476
Alport Syndrome in Women and Girls
@en
P2093
Deb Colville
Frances Flinter
Judy Savige
Moira Finlay
Sharon Lagas
Susie Gear
P2860
P304
P356
10.2215/CJN.00580116
P577
2016-06-10T00:00:00Z