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Hereditary deficiency of phosphoglycerate kinase: a new variant in erythrocytes and leucocytes, not associated with haemolytic anaemia

✍ Scribed by WOLFGANG K. G. KRIETSCH; HELGARD KRIETSCH; WOLFRAM KAISER; MANFRED DUNNWALD; GÜNTER W. K. KUNTZ; JOCHEN DUHM†; THEODOR BÜCHER


Book ID
114725855
Publisher
John Wiley and Sons
Year
1977
Tongue
English
Weight
855 KB
Volume
7
Category
Article
ISSN
0014-2972

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PK MONDOR: PRENATAL DIAGNOSIS OF A FRAME
✍ H. ROUGER; E. GIRODON; M. GOOSSENS; F. GALACTÉROS; M. COHEN-SOLAL 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 767 KB

A mutant form of pyruvate kinase (PK) from the red blood cells of a consanguineous family with severe non-spherocytic haemolytic anaemia has been characterized by polymerase chain reaction (PCR) amplification and sequencing. The variant enzyme was named PK Mondor, according to the recommendations of