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Volumn 37, Issue 10, 2000, Pages
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MPS II in females: molecular basis of two different cases.
a
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
IDURONATE 2 SULFATASE;
MESSENGER RNA;
OUABAIN;
ALLELE;
ANIMAL;
CASE REPORT;
CELL LINE;
CHILD;
CHROMOSOME DELETION;
DNA METHYLATION;
DRUG EFFECT;
ENZYMOLOGY;
FATALITY;
FEMALE;
FIBROBLAST;
FLUORESCENCE IN SITU HYBRIDIZATION;
FRANCE;
GENE EXPRESSION REGULATION;
GENETIC POLYMORPHISM;
GENETICS;
HUMAN;
HUNTER SYNDROME;
HYBRID CELL;
INTRON;
LETTER;
MALE;
METABOLISM;
MUTATION;
PHENOTYPE;
PRESCHOOL CHILD;
RECESSIVE GENE;
SOUTHERN BLOTTING;
X CHROMOSOME;
ALLELES;
ANIMALS;
BLOTTING, SOUTHERN;
CELL LINE;
CHILD;
CHILD, PRESCHOOL;
CHROMOSOME DELETION;
DNA METHYLATION;
DOSAGE COMPENSATION, GENETIC;
FATAL OUTCOME;
FEMALE;
FIBROBLASTS;
FRANCE;
GENES, RECESSIVE;
HUMANS;
HYBRID CELLS;
IDURONATE SULFATASE;
IN SITU HYBRIDIZATION, FLUORESCENCE;
INTRONS;
MALE;
MUCOPOLYSACCHARIDOSIS II;
MUTATION;
OUABAIN;
PHENOTYPE;
POLYMORPHISM, GENETIC;
RNA, MESSENGER;
X CHROMOSOME;
MLCS;
MLOWN;
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EID: 0034298026
PISSN: None
EISSN: 14686244
Source Type: Journal
DOI: 10.1136/jmg.37.10.e29 Document Type: Letter |
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Times cited : (39)
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References (0)
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