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Published in 2020 at "Neurology"
DOI: 10.1212/wnl.0000000000008901
Abstract: Objective Precise genetic analyses were conducted with ring finger protein 213 (RNF213) in relation to a particular clinical phenotype in Chinese patients with moyamoya disease (MMD) to determine whether heterozygosity is responsible for the early-onset…
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Keywords:
phenotype chinese;
rnf213;
phenotype;
r4810k ... See more keywords