Matches in Nanopublications for { ?s ?p "[The most common mutation causing the severe form of CAH is a conversion of an A or C at nucleotide (nt) 656 to a G in the second intron of the steroid 21-hydroxylase gene (CYP21) causing aberrant splicing of mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[The most common mutation causing the severe form of CAH is a conversion of an A or C at nucleotide (nt) 656 to a G in the second intron of the steroid 21-hydroxylase gene (CYP21) causing aberrant splicing of mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP255866.RAgyfYW9NBHtD9XMxvFqcfhTADp8gmYLvS7QLz_3vUmgc130_assertion description "[The most common mutation causing the severe form of CAH is a conversion of an A or C at nucleotide (nt) 656 to a G in the second intron of the steroid 21-hydroxylase gene (CYP21) causing aberrant splicing of mRNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP255866.RAgyfYW9NBHtD9XMxvFqcfhTADp8gmYLvS7QLz_3vUmgc130_provenance.