Found: 2
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Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development.
- Published in:
- Nature Genetics, 2005, v. 37, n. 10, p. 1035, doi. 10.1038/ng1636
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- Article
Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.
- Published in:
- Nature Genetics, 2001, v. 29, n. 3, p. 315, doi. 10.1038/ng744
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- Publication type:
- Article