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High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation
by
E.Neville, Catherine
,
S.Mahadeva, Manl
,
M.Barceló, Juana
,
Korneluk, Robert
Published in
Human molecular genetics
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Human Molecular Genetics
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Base Sequence
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Diseases Of Striated Muscles. Neuromuscular Diseases
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Fragile X Syndrome - Genetics
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