Large genomic deletions: A novel cause of Ullrich congenital muscular dystrophy-Reference-Cited by-同舟云学术

Large genomic deletions: A novel cause of Ullrich congenital muscular dystrophy

Published:2011-01 Issue:1 Volume:69 Page:206-211
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Foley A. Reghan,Hu Ying,Zou Yaqun,Yang Michele,Medne Līvija,Leach Meganne,Conlin Laura K.,Spinner Nancy,Shaikh Tamim H.,Falk Marni,Neumeyer Ann M.,Bliss Laurie,Tseng Brian S.,Winder Thomas L.,Bönnemann Carsten G.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference19 articles.

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2. Microfibrillar Collagen Type VI

3. Type VI Collagen

4. Amino acid sequence of the triple-helical domain of human collagen type VI;Chu;J Biol Chem,1988

5. Sequence analysis of alpha 1(VI) and alpha 2(VI) chains of human type VI collagen reveals internal triplication of globular domains similar to the A domains of von Willebrand factor and two alpha 2(VI) chain variants that differ in the carboxy terminus;Chu;EMBO J,1989

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