𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutational analysis of mitochondrial DNA of children with Rett syndrome

✍ Scribed by Ju Tang; Yu Qi; Xin-Hua Bao; Xi-Ru Wu


Book ID
117591788
Publisher
Elsevier Science
Year
1997
Tongue
English
Weight
807 KB
Volume
17
Category
Article
ISSN
0887-8994

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Mutation analysis of the M6b gene in pat
✍ Narayanan, Vinodh; Olinsky, Shari; Dahle, Elizabeth; Naidu, Sakkubai; Zoghbi, Hu πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 22 KB πŸ‘ 2 views

Human Xp22.2 has been proposed as a candidate region for the Rett syndrome (RTT) gene. M6b, a member of the proteolipid protein gene family, was mapped to Xp22.2 within one of the RTT candidate regions. In this article we describe the structure of the M6b gene, refine the physical mapping of M6b bet