(Q48718783)
Statements
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Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease. (English)
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Suomalainen A
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Majander A
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Wallin M
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Setälä K
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Kontula K
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Leinonen H
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Salmi T
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Paetau A
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Haltia M
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Lonnqvist J
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Peltonen L
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Somer H
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1 May 1997
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48
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5
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1244-1253
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Identifiers
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