Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C) (Q74623416)
Jump to navigation
Jump to search
scientific article published on 01 April 1998
Language | Label | Description | Also known as |
---|---|---|---|
English | Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C) |
scientific article published on 01 April 1998 |
Statements
Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C) (English)
J Brinckmann
Y Açil
S Feshchenko
E Katzer
R Brenner