Homozygous intronic mutation leading to inefficient transcription combined with a novel frameshift mutation in F13A1 gene causes F13 deficiency
スポンサーリンク
概要
著者
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Ma Qiuling
Department Of Biochemistry Hainan Medical College
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Huang Lijun
Department Of Biochemistry Hainan Medical College
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Wang Wei
Department Of Biochemistry Hainan Medical College
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