The α/β- and α2/α1-globin mRNA ratios in different forms of α-thalassemia

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1315, Issue 3, 1996, Pages 188-192

  Smetanina, Natalia S ^a   Leonova, Julia Y ^a   Levy, Norman ^b   Huisman, Titus H J ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

^b DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

Author keywords

Hb H disease; Reverse transcribed polymerase chain reaction; Terminating codon mutation

Indexed keywords

MESSENGER RNA;

ADULT; ALPHA THALASSEMIA; ARTICLE; CASE REPORT; CONTROLLED STUDY; DELETION MUTANT; FEMALE; GENETIC ANALYSIS; HEREDITY; HUMAN; MALE; NEWBORN; PRIORITY JOURNAL; RETICULOCYTE; RNA ANALYSIS;

LAOTIA;

EID: 0029869658     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/0925-4439(95)00123-9     Document Type: Article

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