Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?-Reference-Cited by-同舟云学术

Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?

Published:2018-01 Issue: Volume:106 Page:187-193
ISSN:8756-3282
Container-title:Bone
language:en
Short-container-title:Bone

Author:

Beaufils Camille,Farlay Delphine,Machuca-Gayet Irma,Fassier Alice,Zenker Martin,Freychet Caroline,Bonnelye Edith,Bertholet-Thomas Aurélia,Ranchin Bruno,Bacchetta Justine

Publisher

Elsevier BV

Subject

Histology,Physiology,Endocrinology, Diabetes and Metabolism

Reference43 articles.

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3. Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities;Zenker;Hum. Mol. Genet.,2004

4. Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2);Hinkes;Pediatrics,2007

5. Mutations in the human laminin β2 (LAMB2) gene and the associated phenotypic spectrum;Matejas;Hum. Mutat.,2010

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