Abnormal Dermal Proteoglycan in Aspartylglycosaminuria: A Possible Mechanism for Ultrastructural Changes of Collagen Fibrils in a Glycoprotein Storage Disorder-Reference-Cited by-同舟云学术

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Abnormal Dermal Proteoglycan in Aspartylglycosaminuria: A Possible Mechanism for Ultrastructural Changes of Collagen Fibrils in a Glycoprotein Storage Disorder

Published:1987-01 Issue:4 Volume:16 Page:367-376
ISSN:0300-8207
Container-title:Connective Tissue Research
language:en
Short-container-title:Connective Tissue Research

Author:

Näntö-Salonen K.,Larjava H.,Säämanen A.-M.,Heino J.,Penttinen R.,Pelliniemi L. J.,Tammi M.

Publisher

Informa UK Limited

Subject

Cell Biology,Molecular Biology,Orthopedics and Sports Medicine,Biochemistry,Rheumatology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03008208709005621

Reference33 articles.

1. McKusick V. A. Heritable Disorders of Connective Tissue. The C. V. Mosby Co., St Louis 1972; 740–856

2. Aspartylglucosaminuria

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Secondary biochemical and morphological consequences in lysosomal storage diseases;Biochemistry (Moscow);2014-07

2. The Pathology of the Skeleton in Lysosomal Storage Diseases;Pathobiology of Human Disease;2014

3. Extracellular matrix components: An intricate network of possible biomarkers for lysosomal storage disorders?;FEBS Letters;2013-02-26

4. Progressive nature of aspartylglucosaminuria;Acta Paediatrica;2007-01-02

5. Dysmorphic facial features in aspartylglucosaminuria patients and carriers;Clinical Dysmorphology;2004-01

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