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Novel DDR2 mutation identified by whole exome sequencing in a Moroccan patient with spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type. [electronic resource] by
- Mansouri, Maria
- Kayserili, Hülya
- Elalaoui, Siham Chafai
- Nishimura, Gen
- Iida, Aritoshi
- Lyahyai, Jaber
- Miyake, Noriko
- Matsumoto, Naomichi
- Sefiani, Abdelaziz
- Ikegawa, Shiro
Producer: 20161025
In:
American journal of medical genetics. Part A vol. 170A
Availability: No items available.
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