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[期刊论文] 作者:Pepe G,Lucarini L,周永,, 来源:世界核心医学期刊文摘(神经病学分册) 年份:2006
We have identified highly similar heterozygous COL6A1 genomic deletions, spanning from intron 8 to exon 13 or intron 13, in two patients with Ullrich congenital...
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