Glomerulopathy associated with predominant fibronectin deposits: Exclusion of the genes for fibronectin, villin and desmin as causative genes-Reference-Cited by-同舟云学术

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Glomerulopathy associated with predominant fibronectin deposits: Exclusion of the genes for fibronectin, villin and desmin as causative genes

Published:1996-05-03 Issue:1 Volume:63 Page:323-327
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Hildebrandt Friedhelm,Strahm Brigitte,Prochoroff André,Cybulla Markus,Gemperle Oliver,Krapf Reto,Brandis Matthias

Publisher

Wiley

Subject

Genetics (clinical)

Reference13 articles.

1. Familial lobular glomerulopathy

2. Familial glomerulopathy with giant fibrillar deposits

3. Integrated human genome–wide maps constructed using the CEPH reference panel

4. , and , (1994): A linkage map of human chromosome 2. In: , , , , , , , , , , , , , , , , , , , (eds): “Report of the Third International Workshop on hHuman Chromosome 2 mapping 1994”. Cytogenet Call Genet 67: 215–244 (abstract 5).

5. Genetic renal diseases in children

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