about
Whole exome sequencing reveals novel COL4A3 and COL4A4 mutations and resolves diagnosis in Chinese families with kidney diseaseGlomerular pathology in Alport syndrome: a molecular perspective.Challenge in pathologic diagnosis of Alport syndrome: evidence from correction of previous misdiagnosis.Temporal macular thinning associated with X-linked Alport syndrome.X-linked, COL4A5 hypomorphic Alport mutations such as G624D and P628L may only exhibit thin basement membrane nephropathy with microhematuria and late onset kidney failure.Molecular genetics of familial hematuric diseases.The interface of genetics with pathology in alport nephritis.
P2860
Q34517419-6AC0D4E1-D8F2-41F0-917E-4EFCFFFD92C7Q36359599-852CA070-B958-485F-82AA-DE0C1F075FAAQ36556406-8CC4BFCA-FA4E-45F2-9CCB-A723689E5DFEQ37101426-A3411A2D-F46C-4C15-931D-F5FE843A187BQ37413366-687278EF-3FCA-4A32-A0C9-0D6402E4AEE8Q38138908-5CF802E0-8ACD-4951-82E4-67B02966048AQ42870018-CC48A1DA-69B3-4655-B22D-D3171A4B0B6E
P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Molecular testing for adult type Alport syndrome
@ast
Molecular testing for adult type Alport syndrome
@en
type
label
Molecular testing for adult type Alport syndrome
@ast
Molecular testing for adult type Alport syndrome
@en
prefLabel
Molecular testing for adult type Alport syndrome
@ast
Molecular testing for adult type Alport syndrome
@en
P2093
P2860
P356
P1433
P1476
Molecular testing for adult type Alport syndrome
@en
P2093
Chris Miller
Elaine Lyon
Friederike Gedge
Genevieve Pont-Kingdon
Joyce Denison
Kelli Sumner
Martin Gregory
P2860
P2888
P356
10.1186/1471-2369-10-38
P577
2009-11-17T00:00:00Z
P5875
P6179
1043592223