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Analbuminemia in a Swiss family is caused by a C → T transition at nucleotide 4446 of the albumin gene

✍ Scribed by Monica Campagnoli; Alberto Sala; Sara Labò; Antonio Rossi; Thomas J. Neuhaus; Christian P. Braegger; Lorenzo Minchiotti; Monica Galliano

Book ID
108095312
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
168 KB
Volume
38
Category
Article
ISSN
0009-9120

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Hemoglobin M Iwate is caused by a C→T tr
Hemoglobin M Iwate is caused by a C→T transition in codon 87 of the human α1-globin gene
✍ J. Horst; G. Assum; E. U. Griese; A. Eigel; W. Hampl; E. Kohne 📂 Article 📅 1987 🏛 Springer 🌐 English ⚖ 473 KB

DNA restriction, molecular cloning, and sequencing methods have been used to characterize the mutation leading to the methemoglobinemia HbM Iwate. It could be demonstrated that the HbM Iwate defect is caused by a point mutation involving a transition from C to T in the first position of codon 87 of