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  1. 1
    "NEDO human cDNA sequencing project focused on splicing variants."
    Wakamatsu A., Yamamoto J., Kimura K., Ishii S., Watanabe K., Sugiyama A., Murakawa K., Kaida T., Tsuchiya K., Fukuzumi Y., Kumagai A., Oishi Y., Yamamoto S., Ono Y., Komori Y., Yamazaki M., Kisu Y., Nishikawa T.
    , Sugano S., Nomura N., Isogai T.
    Submitted (OCT-2007) to the EMBL/GenBank/DDBJ databases
    Cited for: NUCLEOTIDE SEQUENCE.
    Category: Sequences.
    Tissue: Brain.
    Source: UniProtKB/TrEMBL (unreviewed).
  2. 2
    Category: Sequences.
    Source: UniProtKB/TrEMBL (unreviewed).

    This publication is cited by 1021 other entries.

  3. 3
    "Association of nonsense mutation of dystrophin gene with disruption of sarcoglycan complex in X-linked dilated cardiomyopathy."
    Franz W.M., Muller M., Muller O.J., Herrmann R., Rothmann T., Cremer M., Cohn R.D., Voit T., Katus H.A.
    Lancet 355:1781-1785(2000) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with CARDIOVASCULAR: X-linked dilated cardiomyopathy.Imported.
    Source: GAD:139353.

    This publication is mapped to 80 other entries.

  4. 4
    "Mutations in the dystrophin gene are associated with sporadic dilated cardiomyopathy."
    Feng J., Yan J., Buzin C.H., Towbin J.A., Sommer S.S.
    Mol. Genet. Metab. 77:119-126(2002) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with CARDIOVASCULAR: dilated cardiomyopathy.Imported.
    Source: GAD:139355.

    This publication is mapped to 79 other entries.

  5. 5
    "Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy."
    Nishiyama A., Takeshima Y., Saiki K., Narukage A., Oyazato Y., Yagi M., Matsuo M.
    BMC Med. Genet. 8:19-19(2007) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Not Associated with DEVELOPMENTAL: muscular dystrophy.Imported.
    Source: GAD:146734.

    This publication is mapped to 80 other entries.

  6. 6
    "Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy."
    Rapaport D., Passos-Bueno M.R., Brandao L., Love D., Vainzof M., Zatz M.
    Am. J. Med. Genet. 39:437-441(1991) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with OTHER: Duchenne muscular dystrophy.Imported.
    Source: GAD:139352.

    This publication is mapped to 80 other entries.

  7. 7
    "Novel small mutations along the DMD/BMD gene associated with different phenotypes."
    Nigro V., Nigro G., Esposito M.G., Comi L.I., Molinari A.M., Puca G.A., Politano L.
    Hum. Mol. Genet. 3:1907-1908(1994) [PubMed] [Europe PMC] [Abstract]
    Category: Pathology & Biotech.
    Annotation: Associated with OTHER: muscular dystrophy.Imported.
    Source: GAD:139351.

    This publication is mapped to 79 other entries.

1 to 7 of 7  Show

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