Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice (Q28511659)

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Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice
scientific journal article

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    title
    Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral response in mice (English)
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    author name string
    Subramaniam Ganesh
    series ordinal
    1
    1 reference
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    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Antonio V. Delgado-Escueta
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    2
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Toshiro Sakamoto
    series ordinal
    3
    1 reference
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    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Maria Rosa Avila
    series ordinal
    4
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
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    25 January 2017
    Jesus Machado-Salas
    series ordinal
    5
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Yoshinobu Hoshii
    series ordinal
    6
    1 reference
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    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Takumi Akagi
    series ordinal
    7
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Hiroshi Gomi
    series ordinal
    8
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Toshimitsu Suzuki
    series ordinal
    9
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Kenji Amano
    series ordinal
    10
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Kishan Lal Agarwala
    series ordinal
    11
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Yuki Hasegawa
    series ordinal
    12
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Dong-Sheng Bai
    series ordinal
    13
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Tokuhiro Ishihara
    series ordinal
    14
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Tsutomu Hashikawa
    series ordinal
    15
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Shigeyoshi Itohara
    series ordinal
    16
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Eain M. Cornford
    series ordinal
    17
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Hiroaki Niki
    series ordinal
    18
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    Kazuhiro Yamakawa
    series ordinal
    19
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
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    25 January 2017
    publication date
    15 May 2002
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    volume
    11
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    issue
    11
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017
    page(s)
    1251–1262
    1 reference
    stated in
    PubMed
    PubMed ID
    12019206
    retrieved
    25 January 2017

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