Deletion of Exons 3 through 5 of ABCG2 causes the Jr(a−) phenotype in a West African woman

Publisher： John Wiley & Sons Inc

E-ISSN： 1537-2995|55|11|2766-2767

ISSN： 0041-1132

Source： TRANSFUSION, Vol.55, Iss.11, 2015-11, pp. : 2766-2767

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

A new ABCG2 null allele with a 27‐kb deletion including the promoter region causing the Jr(a−) phenotype

By  

TRANSFUSION, Vol. 55, Iss. 6pt2, 2015-06 ,pp. : 1467-1471

John Wiley & Sons Inc

Access to resources Recommend Favorite

MFN2 deletion of exons 7 and 8: founder mutation in the UK population

By  

JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, Vol. 20, Iss. 2, 2015-06 ,pp. : 67-71

John Wiley & Sons Inc

Access to resources Recommend Favorite

Griscelli syndrome type 3‐like phenotype with MYO‐5A exon‐F deletion

By  

PEDIATRIC ALLERGY AND IMMUNOLOGY, Vol. 25, Iss. 8, 2014-12 ,pp. : 817-819

John Wiley & Sons Inc

Access to resources Recommend Favorite

Angelman Syndrome due to a Maternally Inherited Intragenic Deletion Encompassing Exons 7 and 8 of the UBE3A Gene

By  

Cytogenetic and Genome Research, Vol. 152, Iss. 3, 2017-09 ,pp. : 132-136

Karger

Access to resources Recommend Favorite

An ATP-binding cassette gene (ABCG5) from the ABCG (White) gene subfamily maps to human chromosome 2p21 in the region of the Sitosterolemia locus

By  

Cytogenetic and Genome Research, Vol. 92, Iss. 3-4, 2001-06 ,pp. : 204-208

Karger

Access to resources Recommend Favorite