Aspartylglucosaminuria: unusual neonatal presentation in qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family
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| Other Authors: | , , , , , , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
2014
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| In: |
Journal of child neurology
Year: 2014, Volume: 29, Issue: 1, Pages: 36-42 |
| ISSN: | 1708-8283 |
| DOI: | 10.1177/0883073812469049 |
| Online Access: | Verlag, kostenfrei, Volltext: http://dx.doi.org/10.1177/0883073812469049
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| Author Notes: | Opladen, Thomas; Ebinger, Friedrich; Zschocke, Johannes; Sengupta, Devjani; Ben-Omran, Tawfeg; Shahbeck, Noora; Moog, Ute; Fischer, Christine; Buerger, Friederike; Haas, Dorothea; Ruef, Peter; Harting, Inga; Al-Rifai, Hilal; Hoffmann, Georg F. |
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