✦ LIBER ✦
Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation
✍ Scribed by Tri Wibawa; Yasuhiro Takeshima; Izuru Mitsuyoshi; Hiroko Wada; Agus Surono; Hajime Nakamura; Masafumi Matsuo
- Book ID
- 117545974
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 231 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0387-7604
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