Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation.
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Accession number;00A0486853
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| Title;Complete skipping of exon 66 due to novel mutations of the dystrophin gene was identified in two Japanese families of Duchenne muscular dystrophy with severe mental retardation. |
| Author;
WIBAWA T
(Kobe Univ. School Of Medicine, Kobe, Jpn)
TAKESHIMA Y
(Kobe Univ. School Of Medicine, Kobe, Jpn)
MITSUYOSHI I
(National Utano Hospital, Kyoto, Jpn)
WADA H
(Sakura Ryoikuen Hospital, Sanda, Jpn)
SURONO A
(Kobe Univ. School Of Medicine, Kobe, Jpn)
NAKAMURA H
(Kobe Univ. School Of Medicine, Kobe, Jpn)
MATSUO M
(Kobe Univ. School Of Medicine, Kobe, Jpn)
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Journal Title;Brain & Dev
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Journal Code:W0814A
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ISSN:0387-7604
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VOL.22;NO.2;PAGE.107-112(2000)
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| Figure&Table&Reference;FIG.5, REF.34 |
| Pub. Country;Netherlands |
| Language;English |
| Abstract; |
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