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Volumn 58, Issue 6, 1996, Pages 1135-1144
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Mutational and protein analysis of patients and heterozygous women with X- linked adrenoleukodystrophy
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Author keywords
[No Author keywords available]
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Indexed keywords
ABC TRANSPORTER;
DNA;
VERY LONG CHAIN FATTY ACID;
ADRENOLEUKODYSTROPHY;
ARTICLE;
DEGENERATIVE DISEASE;
DEMYELINATING DISEASE;
FAMILY STUDY;
FATTY ACID OXIDATION;
FIBROBLAST CULTURE;
GENE MUTATION;
HUMAN;
HUMAN CELL;
LYMPHOCYTE CULTURE;
PRIORITY JOURNAL;
PROTEIN ANALYSIS;
X CHROMOSOME INACTIVATION;
X CHROMOSOME LINKED DISORDER;
ADDISON DISEASE;
ADOLESCENT;
ADRENOLEUKODYSTROPHY;
ALTERNATIVE SPLICING;
AMINO ACID SEQUENCE;
ATP-BINDING CASSETTE TRANSPORTERS;
BASE SEQUENCE;
CHILD;
CHILD, PRESCHOOL;
DNA;
DNA PRIMERS;
ELECTROPHORESIS;
EXONS;
FEMALE;
FIBROBLASTS;
FRAMESHIFT MUTATION;
HETEROZYGOTE DETECTION;
HUMANS;
LEUKOCYTES;
MALE;
MEMBRANE PROTEINS;
MOLECULAR SEQUENCE DATA;
POINT MUTATION;
POLYMERASE CHAIN REACTION;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
X CHROMOSOME;
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EID: 0029932863
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (96)
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References (0)
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