Ehlers-Danlos syndrome type VI: lysyl hydroxylase deficiency due to a novel point mutation (W612C)
J. Brinckmann, Yahya Açil, Sergej Feshchenko, Eva Katzer, Rolf Brenner, Andreas Kulozik, Sebastian KüglerVolume:
290
Language:
english
Pages:
6
DOI:
10.1007/s004030050287
Date:
May, 1998
File:
PDF, 125 KB
english, 1998