Population
45 British families with facioscapulohumeral muscular dystrophy
Design
Other
Authors
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May support FSHD genetic testing; extends linkage data but leaves clinical adoption open.
The DNA marker p13E-11 is closely linked to facioscapulohumeral muscular dystrophy and detects de novo DNA rearrangements associated with the disease.
Upadhyaya et al. (1993) studied this question.
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