Literature DB >> 20642652

C1q nephropathy associated with deletion of long arm of chromosome 7.

Agnieshka Judkins, Sharron Townshend, Frank Willis.   

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Year:  2010        PMID： 20642652     DOI： 10.1111/j.1440-1754.2010.01785.x

Source DB:  PubMed          Journal:  J Paediatr Child Health        ISSN： 1034-4810            Impact factor:   1.954


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  2 in total

1.  Is C1q nephropathy associated with a WDR19 gene mutation? A case report.

Authors:  K Kaynar; B Güvercin; Ö Güler; S Mungan; E Çağlayan
Journal:  Hippokratia       Date:  2021 Apr-Jun       Impact factor: 0.522

2.  C1q nephropathy in adults is a form of focal segmental glomerulosclerosis in terms of clinical characteristics.

Authors:  Kipyo Kim; Hyung-Eun Son; Ji-Young Ryu; Hajeong Lee; Seung Hyeok Han; Dong-Ryeol Ryu; Jin Ho Paik; Sejoong Kim; Ki Young Na; Dong-Wan Chae; Ho Jun Chin; Se Won Oh
Journal:  PLoS One       Date:  2019-04-19       Impact factor: 3.240
  2 in total

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