Erythroid urea transporter deficiency due to novel JKnull alleles

Transfusion

Volumn 48, Issue 2, 2008, Pages 365-372

  Wester, Elisabet S ^b   Johnson, Susan T ^b   Copeland, Tama ^b   Malde, Ranjan ^b   Lee, Edmond ^b   Storry, Jill R ^a   Olsson, Martin L ^b  

^a LUND UNIVERSITY HOSPITAL   (Sweden)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPROTEIN; THREONINE;

AFRICAN AMERICAN; ALLELE; ARTICLE; ERYTHROCYTE; ERYTHROCYTE MEMBRANE; ERYTHROID UREA TRANSPORTER DEFICIENCY; FEMALE; GENE; GENE AMPLIFICATION; GENE IDENTIFICATION; GENE MUTATION; GENETIC ANALYSIS; GENETIC DISORDER; HUMAN; IMMUNOBLOTTING; INDIAN; JK GENE; MALE; MOTHER; NONSENSE MUTATION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; WESTERN BLOTTING;

ALLELES; BASE SEQUENCE; ERYTHROID CELLS; GENOME, HUMAN; HUMANS; INTRONS; KIDD BLOOD-GROUP SYSTEM; MEMBRANE TRANSPORT PROTEINS; MUTATION;

EID: 38349184783     PISSN: 00411132     EISSN: 15372995     Source Type: Journal    
DOI: 10.1111/j.1537-2995.2007.01532.x     Document Type: Article

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