## Abstract **BACKGROUND:**__PAX3__ plays an important role in mammalian embryonic development. Known mutations in __PAX3__ are etiologically associated with Waardenburg syndrome and syndromic neural tube defects (NTDs). Mutations in the murine homologue, __pax3__, are responsible for the phenotype
Loss of function polymorphisms inNAT1protect against spina bifida
β Scribed by Liselotte E. Jensen; Karen Hoess; Laura E. Mitchell; Alexander S. Whitehead
- Publisher
- Springer
- Year
- 2006
- Tongue
- English
- Weight
- 194 KB
- Volume
- 120
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
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