On the significance of isolated exclusions in the PGM1 subtype system
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-73330-7_20.pdf
Reference22 articles.
1. Bertrams J, Hintzen U, Barberan F (1986) A new partially deficient variant in the phosphoglucomutase 1 system, PGM*W31. Hum. Genet. 72: 177–178
2. Brinkmann B, Koops E, Klopp O, Heindl K (1972) Inherited partial deficiency of the PGM 11 11 gene: biochemical and densitometric studies. Ann Hum Genet Lond 35: 363–366
3. Brinkmann B, Riemann U, Heide KG, Sachs W, Walcher A, Heindl K, Hoppe H (1973) Demonstration of the silent allele PGM O1 O1 in three families and description of a new variant. Z. Rechtsmedizin 73: 207–217
4. Driesel AJ, Basler M, Henke J (1982) PGM a1 a1 subtyping in Western Germany (Düsseldorf region). Z Rechtsmed 88: 313–316
5. Dykes DD, Copouls BA, Polesky HF (1982) Routine phenotyping of phosphoglucomutase (PGM1) by thinlayer focusing: Isoelectric points of 14 different variants. Electrophoresis 3: 165–168
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1. Mapping Recombination Hotspots in Human Phosphoglucomutase (PGM1);Human Molecular Genetics;1999-09-01
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