(Q74122663)
Statements
A compound heterozygote patient with Ehlers-Danlos syndrome type VI has a deletion in one allele and a splicing defect in the other allele of the lysyl hydroxylase gene (English)
Pousi B
Hautala T
Hyland JC
Schröter J
Eckes B
Kivirikko KI
1 January 1998