Exon 2 was replaced with a mutant exon 2 encoding an R48C substitution, linked to heterozygous type II HBS deficiency patients, and an additional silent mutation creating a SacI site. (J:115658)
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Exon 2 was replaced with a mutant exon 2 encoding an R48C substitution, linked to heterozygous type II HBS deficiency patients, and an additional silent mutation creating a SacI site. (J:115658)