| 000 | nab a22 7a 4500 | ||
|---|---|---|---|
| 999 |
_c16884 _d16884 |
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| 003 | PC16884 | ||
| 005 | 20220601131505.0 | ||
| 008 | 220601b xxu||||| |||| 00| 0 eng d | ||
| 040 | _cH12O | ||
| 041 | _aeng | ||
| 100 |
_91007 _aArenas Barbero, Joaquín _eInstituto de Investigación |
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| 100 |
_93056 _aMartín, Miguel Ángel _eInstituto de investigación imas12 |
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| 100 |
_92420 _aMartinez Azorin, Francisco _eInstituto de Investigación i+12 |
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| 245 | 0 | 0 |
_aCongenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. _h[caso clínico] |
| 260 |
_bBrain & development, _c2016 |
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| 300 | _a38(1):167-72. | ||
| 500 | _aFormato Vancouver: Castro Gago M, Dacruz Alvárez D, Pintos Martínez E, Beiras Iglesias A, Arenas J, Martín MÁ et al. Congenital neurogenic muscular atrophy in megaconial myopathy due to a mutation in CHKB gene. Brain Dev. 2016 Jan;38(1):167-72. | ||
| 501 | _aPMID: 26006750 | ||
| 504 | _aContiene 20 referencias | ||
| 710 |
_9625 _aInstituto de Investigación imas12 |
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| 856 |
_uhttp://pc-h12o-es.m-hdoct.a17.csinet.es/pdf/pc/1/pc16884.pdf _ySolicitar documento |
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| 942 |
_2ddc _cCAS _n0 |
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