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Nature Genetics|August 4, 1999
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiencyA Brooks-Wilson, M Marcil, S M Clee, et al.
Clinical Genetics|May 2, 2007
Loss-of-function mutations in the Nav1.7 gene underlie congenital indifference to pain in multiple human populationsY P Goldberg, J MacFarlane, M L MacDonald, et al.
Neurology|February 11, 2012
CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashionJ-M Lee, E M Ramos, J-H Lee, et al.
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