Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins

✍ Scribed by Gregory M. Enns; Robert D. Steiner; Neil Buist; Charles Cowan; Kathleen A. Leppig; Marjorie F. McCracken; Vibeke Westphal; Hudson H. Freeze; John F. O'Brien; Jaak Jaeken; Gert Matthijs; Sarina Behera; Louanne Hudgins

• Book ID: 117848244
• Publisher: Elsevier Science
• Year: 2002
• Tongue: English
• Weight: 122 KB
• Volume: 141
• Category: Article
• ISSN: 1097-6833
• DOI: 10.1067/mpd.2002.128658