Kühnl P, Anneken K, Spielmann W
Hum Genet. 1979 Mar 12;47(2):187-91. doi: 10.1007/BF00273200.
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.