Related Experiment Videos

Collagen biosynthesis in human skin. A review with emphasis on scleroderma

Annals of Clinical Research

|October 1, 1971

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

Epidermolysis bullosa: novel and de novo premature termination codon and deletion mutations in the plectin gene predict late-onset muscular dystrophy.

The Journal of investigative dermatology·2000

Mutation reports: epidermolysis bullosa simplex associated with severe mucous membrane involvement and novel mutations in the plectin gene.

The Journal of investigative dermatology·2000

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

Experimental eye research·2000

Compound heterozygosity for novel splice site mutations in the BPAG2/COL17A1 gene underlies generalized atrophic benign epidermolysis bullosa.

The Journal of investigative dermatology·2000

Cutaneous gene therapy. Principles and prospects.

Dermatologic clinics·2000

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy.

American journal of ophthalmology·1999

See all related articles