Literature DB >> 1132880

A homozygote for a serum albumin variant of the slow type.

C Petrini, F Giorcelli, F Porta, M Fraccaro.   

Abstract

A woman from the Trento district of Northern Italy was found to have albumin of a variant type only. Her parents were first cousins and she had two daughters who were both alloalbuminemic. This is probably the first case of a homozygote for a slow albumin variant and it indicates that individuals with only electrophoretically unusual albumin are physiologically normal.

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Year:  1975        PMID： 1132880     DOI： 10.1007/bf00281459

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


  4 in total

1.  [Variants of serum albumin in 22 families compared by means of electrophoresis].

Authors:  F Porta; P Boccato; L Bonazzi; E Bozzetti; A Burlina; F Fisauli; L Galzigna; M Marinucci; V Ortali; C Petrini; G Ruffini; L Tentori
Journal:  Boll Ist Sieroter Milan       Date:  1973 Jan-Feb

2.  Human serum albumin: twenty-three genetic variants and their population distribution.

Authors:  L R Weitkamp; F M Salzano; J V Neel; F Porta; R A Geerdink; A L Tárnoky
Journal:  Ann Hum Genet       Date:  1973-04       Impact factor: 1.670

3.  [Alloalbuminemia (bisalbuminemia) of the slow type].

Authors:  F Porta; G Ruffini; M Pasino; A Scherini
Journal:  Minerva Med       Date:  1972-03-24       Impact factor: 4.806

4.  Albumin polymorphism in man. Studies on albumin variants in North American native populations.

Authors:  L Melartin
Journal:  Acta Pathol Microbiol Scand       Date:  1967
  4 in total
  2 in total

1.  Human albumin genetic variants: an attempt at a classification of European allotypes.

Authors:  J M Fine; M Marneux; D Rochu
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

2.  A homozygote for a serum albumin variant of the fast type.

Authors:  G Vanzetti; F Porta; L Prencipe; A Scherini; M Fraccaro
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132
  2 in total

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