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Volumn 46, Issue 4, 1996, Pages 1189-1190
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Pattern of X-chromosome inactivation as a key determinant of the clinicopathologic phenotype of Duchenne muscular dystrophy carriers
a a
a
NONE
(Canada)
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Author keywords
[No Author keywords available]
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Indexed keywords
ANIMAL;
ANIMAL MUSCULAR DYSTROPHY;
FEMALE;
GENETICS;
HETEROZYGOTE;
HUMAN;
MALE;
MOUSE;
MUSCULAR DYSTROPHY;
NOTE;
PHENOTYPE;
X CHROMOSOME;
X CHROMOSOME LINKED MUSCULAR DYSTROPHIC MOUSE;
ANIMALS;
FEMALE;
HETEROZYGOTE;
HUMANS;
MALE;
MICE;
MICE, INBRED MDX;
MUSCULAR DYSTROPHIES;
MUSCULAR DYSTROPHY, ANIMAL;
PHENOTYPE;
X CHROMOSOME;
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EID: 0030118246
PISSN: 00283878
EISSN: 1526632X
Source Type: Journal
DOI: 10.1212/WNL.46.4.1189-b Document Type: Letter |
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Times cited : (4)
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References (0)
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