Kelley–Seegmiller syndrome due to a new variant of the hypoxanthine–guanine phosphoribosyltransferase (I136T) encoding gene (HPRT Marseille)

✍ Scribed by B. Dussol; I. Ceballos-Picot; B. Aral; V. Castera; N. Philip; Y. Berland

• Book ID: 111574766
• Publisher: Springer
• Year: 2004
• Tongue: English
• Weight: 50 KB
• Volume: 27
• Category: Article
• ISSN: 0141-8955
• DOI: 10.1023/b:boli.0000037399.72152.a9