✦ LIBER ✦
Niemann-Pick C1 Disease: The I1061T Substitution Is a Frequent Mutant Allele in Patients of Western European Descent and Correlates with a Classic Juvenile Phenotype
✍ Scribed by Gilles Millat; Christophe Marçais; Mohammad A. Rafi; Toshiyuki Yamamoto; Jill A. Morris; Peter G. Pentchev; Kousaku Ohno; David A. Wenger; Marie T. Vanier
- Book ID
- 117853044
- Publisher
- American Society of Human Genetics
- Year
- 1999
- Tongue
- English
- Weight
- 133 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/302626
No coin nor oath required. For personal study only.