A cysteine for glycine substitution at position 1017 in an α1(I) chain of type I collagen in a patient with mild dominantly inherited osteogenesis imperfecta

M. E. Labhard, Mary Wirtz, F. M. Pope, A. C. Nicholls, D. W. Hollister

Research output: Contribution to journalArticle

6 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)197-207
Number of pages11
JournalMolecular Biology and Medicine
Volume5
Issue number3
StatePublished - 1988

Fingerprint

Osteogenesis Imperfecta
Peptide Fragments
Molecular Cloning
Collagen Type I
Glycine
Cysteine
Amino Acid Sequence
Collagen
Mutation

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics(clinical)

Cite this

A cysteine for glycine substitution at position 1017 in an α1(I) chain of type I collagen in a patient with mild dominantly inherited osteogenesis imperfecta. / Labhard, M. E.; Wirtz, Mary; Pope, F. M.; Nicholls, A. C.; Hollister, D. W.

In: Molecular Biology and Medicine, Vol. 5, No. 3, 1988, p. 197-207.

Research output: Contribution to journalArticle

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