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Volumn 40, Issue 5, 1996, Pages 693-694
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Autosomal dominant chronic progressive external ophthalmoplegia: A tale of two genomes
a
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Author keywords
[No Author keywords available]
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Indexed keywords
AUTOSOMAL DOMINANT DISORDER;
DISEASE ASSOCIATION;
DNA DETERMINATION;
EDITORIAL;
GENE DELETION;
GENETIC HETEROGENEITY;
HUMAN;
KEARNS SAYRE SYNDROME;
OPHTHALMOPLEGIA;
PRIORITY JOURNAL;
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EID: 0029844433
PISSN: 03645134
EISSN: None
Source Type: Journal
DOI: 10.1002/ana.410400503 Document Type: Editorial |
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Times cited : (9)
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References (0)
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