| Literature DB >> 86494 |
P Kühnl, K Anneken, W Spielmann.
Abstract
A rare peptidase A variant, tentatively designated PEP A9, was observed in six members of a German family, indicating autosomal codominant inheritance. The electrophoretic mobility is similar to that of PEP A 3-1, but it has very low in vivo stability. There is no apparent association with a disease state. A simple and sensitive staining reagent for PEP A was found in o-phthalaldehyde.Entities:
Mesh:
Substances:
Year: 1979 PMID: 86494 DOI: 10.1007/BF00273200
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132