✦ LIBER ✦
Two novel mutations in SLC6A8 cause creatine transporter defect and distinctive X-linked mental retardation in two unrelated Dutch families
✍ Scribed by G.M.S. Mancini; C.E. Catsman-Berrevoets; I.F.M. de Coo; F.K. Aarsen; J.H.J. Kamphoven; J.G. Huijmans; M. Duran; M.S. van der Knaap; C. Jakobs; G.S. Salomons
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 356 KB
- Volume
- 132A
- Category
- Article
- ISSN
- 1552-4825
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