Literature DB >> 32258238

A Novel XK Gene Mutation Causative of McLeod Syndrome.

Priya Srikanth1, Omar A Al-Louzi1, Michael P Bowley1, Aleksandar Videnovic1.   

Abstract

Entities:  

Keywords:  McLeod; XK; chorea; neuroacanthocytosis

Year:  2020        PMID： 32258238      PMCID： PMC7111571          DOI： 10.1002/mdc3.12912

Source DB:  PubMed          Journal:  Mov Disord Clin Pract        ISSN： 2330-1619


× No keyword cloud information.
  3 in total

1.  Protein 4.1R-dependent multiprotein complex: new insights into the structural organization of the red blood cell membrane.

Authors:  Marcela Salomao; Xihui Zhang; Yang Yang; Soohee Lee; John H Hartwig; Joel Anne Chasis; Narla Mohandas; Xiuli An
Journal:  Proc Natl Acad Sci U S A       Date:  2008-06-04       Impact factor: 11.205

Review 2.  Molecular Basis and Clinical Overview of McLeod Syndrome Compared With Other Neuroacanthocytosis Syndromes: A Review.

Authors:  Eileen Roulis; Catherine Hyland; Robert Flower; Christoph Gassner; Hans H Jung; Beat M Frey
Journal:  JAMA Neurol       Date:  2018-12-01       Impact factor: 18.302

3.  Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.

Authors:  M Ho; J Chelly; N Carter; A Danek; P Crocker; A P Monaco
Journal:  Cell       Date:  1994-06-17       Impact factor: 41.582
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.