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Arteriosclerosis Obliterans
A recessive founder mutation in regulator of telomere elongation helicase 1, RTEL1, underlies severe immunodeficiency and features of Hoyeraal Hreidarsson syndrome.
Carbonic Anhydrase I
Quadriplegia
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Principal Investigator
Overview
researcher role of
Conley, Shannon
contributes to
The role of IGF-1 signaling in vascular smooth muscle cells in age-related vascular cognitive impairment and dementia