ISSN:
1546-1718
Source:
Nature Archives 1869 - 2009
Topics:
Biology
,
Medicine
Notes:
[Auszug] To elucidate the defect in HSS, we took a genetic approach using homozygosity mapping8. Others have used this method to map genes including those for Bardet-Biedl syndrome9, familial Mediterranean fever10, Friedreich's ataxia phenotype with selective vitamin E deficiency11, and Hirschsprung ...
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1038/ng1296-479