Novel nonsense mutation (R194X) in the PMM2 gene in a Japanese patient with congenital disorder of glycosylation type Ia
2003 ◽
Vol 25
(7)
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pp. 525-528
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2006 ◽
Vol 148
(1)
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pp. 115-117
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2001 ◽
Vol 85
(3)
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pp. 236-239
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2008 ◽
Vol 66
(3a)
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pp. 545-548
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2006 ◽
Vol 71
(3)
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pp. 348-353
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2007 ◽
Vol 44
(4)
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pp. 277-280
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2002 ◽
Vol 161
(10)
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pp. 524-527
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