✦ LIBER ✦
A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder
✍ Scribed by Ghada M.H. Abdel-Salam; Noriko Miyake; Maha M. Eid; Mohamed S. Abdel-Hamid; Nihal A. Hassan; Ola M. Eid; Laila K. Effat; Tarek H. El-Badry; Ghada Y. El-Kamah; Mohamed El-Darouti; Naomichi Matsumoto
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 347 KB
- Volume
- 155
- Category
- Article
- ISSN
- 1552-4825
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