The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy (Q28214777)
scientific article (publication date: September 2001)
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Current Data About The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy
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(P1476) "The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy" (language: en)

(P2093) I Eisenberg
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N Avidan
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T Potikha
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H Hochner
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M Chen
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T Olender
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M Shemesh
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M Sadeh
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G Grabov-Nardini
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I Shmilevich
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A Friedmann
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G Karpati
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W G Bradley
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L Baumbach
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E B Asher
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J S Beckmann
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Z Argov
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S Mitrani-Rosenbaum
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other details
description scientific article (publication date: September 2001)

External Links
(P356) 10.1038/NG718
(P698) 11528398
(P3181) 606933
(P5875) 11818405