Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene (Q73734974)
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scientific article published on 01 April 2001
Language | Label | Description | Also known as |
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English | Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene |
scientific article published on 01 April 2001 |
Statements
Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene (English)
Kugler W
Pekrun A
Laspe P
Erdlenbruch B