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607855.3
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Subject Details
Country
Saudi Arabia
HPO Terms
Hypotonia
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Sex
Male
Family History
Yes
Parental Consanguinity
No
Subject Variants
Variant Name
Allele Count
Allele Frequency
Associated Disease
Associated Gene
NM_000426.4:c.1762del
2
Muscular Dystrophy, Congenital Merosin-Deficient, 1A
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