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Journal of Medical Genetics 1991;28:458-463; doi:10.1136/jmg.28.7.458
Copyright © 1991 by the BMJ Publishing Group Ltd.

Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IV.

A J Richards, J C Lloyd, P N Ward, A De Paepe, P Narcisi, F M Pope

Dermatology Research Group, Clinical Research Centre, Northwick Park Hospital, Harrow, Middlesex.

We have studied a patient with Ehlers-Danlos syndrome type IV. Protein mapping studies of her type III collagen had indicated that cyanogen bromide fragment 9 contained the site of the mutation. Here we describe the mapping of this region for a single base mutation using a chemical modification and cleavage technique. Sequence analysis of cDNA showed a G to T mutation resulting in the substitution of glycine 910 by valine. This was confirmed by allele specific oligonucleotide hybridisation to the proband's genomic DNA.


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This article has been cited by other articles:

  • Purohit, N., Marsland, D., Roberts, N., Townsend, E. (2009). Haemo-pneumothorax and haemoptysis in a patient with suspected Ehlers-Danlos syndrome. ICVTS 9: 130-131 [Abstract] [Full Text]  

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