Literature DB >> 4847946

p phenotype in two successive generations of a Japanese family.

S Miwa, T Matuhasi, J Yasuda.   

Abstract

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Year:  1974        PMID： 4847946     DOI： 10.1111/j.1423-0410.1974.tb02733.x

Source DB:  PubMed          Journal:  Vox Sang        ISSN： 0042-9007            Impact factor:   2.144


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  2 in total

1.  P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management.

Authors:  Ashish N Kanani; Snehal B Senjaliya; Manisha M Rajapara; Judith Aeschlimann; Connie M Westhoff; Sanmukh R Joshi
Journal:  Transfus Med Hemother       Date:  2021-02-25       Impact factor: 3.747

2.  Abnormalities in the glycosphingolipid content of human Pk and p erythrocytes.

Authors:  D M Marcus; M Naiki; S K Kundu
Journal:  Proc Natl Acad Sci U S A       Date:  1976-09       Impact factor: 11.205
  2 in total

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