Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlap
Keyword(s):
2000 ◽
Vol 48
(2)
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pp. 143-150
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Keyword(s):
1994 ◽
Vol 57
(12)
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pp. 1545-1546
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Keyword(s):
2001 ◽
Vol 9
(4)
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pp. 311-315
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