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Aspartylglucosaminuria: unusual neonatal presentation in Qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family. [electronic resource] by
- Opladen, Thomas
- Ebinger, Friedrich
- Zschocke, Johannes
- Sengupta, Devjani
- Ben-Omran, Tawfeg
- Shahbeck, Noora
- Moog, Ute
- Fischer, Christine
- Bürger, Friederike
- Haas, Dorothea
- Ruef, Peter
- Harting, Inga
- Al-Rifai, Hilal
- Hoffmann, Georg F
Producer: 20140829
In:
Journal of child neurology vol. 29
Availability: No items available.
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