Mutation of a highly conserved residue of βI spectrin associated with fatal and near-fatal neonatal hemolytic anemia

Journal of Clinical Investigation

Volumn 99, Issue 2, 1997, Pages 267-277

  Gallagher, Patrick G ^a   Petruzzi, Mary Jane ^b   Weed, Scott A ^a   Zhang, Zhushan ^a   Marchesi, Sally L ^a   Mohandas, Narla ^c   Morrow, Jon S ^a   Forget, Bernard G ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL OF BUFFALO   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

membrane skeleton; molecular modeling; mutation; skeletal muscle; spectrin

Indexed keywords

SPECTRIN;

AMINO ACID ANALYSIS; AMINO ACID SEQUENCE; ARTICLE; DISEASE ASSOCIATION; DROSOPHILA; ERYTHROCYTE TRANSFUSION; FETUS HYDROPS; GENE MUTATION; HEMOLYTIC ANEMIA; HUMAN; HUMAN CELL; HYDROPHOBICITY; IMMUNOHISTOCHEMISTRY; NEWBORN; PRIORITY JOURNAL; SKELETAL MUSCLE;

EID: 0031017565     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI119155     Document Type: Article

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