Thomas Hollis to Basal Ganglia Diseases
This is a "connection" page, showing publications Thomas Hollis has written about Basal Ganglia Diseases.
Connection Strength
0.073
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Rice G, Newman WG, Dean J, Patrick T, Parmar R, Flintoff K, Robins P, Harvey S, Hollis T, O'Hara A, Herrick AL, Bowden AP, Perrino FW, Lindahl T, Barnes DE, Crow YJ. Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome. Am J Hum Genet. 2007 Apr; 80(4):811-5.
Score: 0.073