COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture-Reference-Cited by-同舟云学术

COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular rupture

Published:1996-08 Issue:2 Volume:135 Page:163-181
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:

Author:

POPE F. M.,NARCISl P.,NICHOLLS A.C.,GERMAINE D.,PALS G.,RICHARDS A. J.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.1996.tb01143.x/fullpdf

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3. Ehlers-Dablos syndrome type VII: a single base change that causes exon skipping in the type I collagen alpha 2(1) chain;Nicholls;Hum Genet,1991

4. Evidence for a relationship between Ehlers-Danlos type VIIC in human and bovine dermatosporaxis;Nusgens;Nat Genet,1992

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