| 000 | 01133 a2200325 4500 | ||
|---|---|---|---|
| 005 | 20250513034850.0 | ||
| 264 | 0 | _c19950911 | |
| 008 | 199509s 0 0 eng d | ||
| 022 | _a0006-291X | ||
| 024 | 7 |
_a10.1006/bbrc.1995.2139 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aLin, C Y | |
| 245 | 0 | 0 |
_aIdentification of a de Novo point mutation resulting in infantile form of Pompe's disease. _h[electronic resource] |
| 260 |
_bBiochemical and biophysical research communications _cAug 1995 |
||
| 300 |
_a367 p. _bdigital |
||
| 500 | _aPublication Type: Published Erratum | ||
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aAspartic Acid |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 | _aCodon |
| 650 | 0 | 4 |
_aGlycogen Storage Disease Type II _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aInfant |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 | _aPoint Mutation |
| 650 | 0 | 4 |
_aalpha-Glucosidases _xgenetics |
| 700 | 1 | _aShieh, J J | |
| 773 | 0 |
_tBiochemical and biophysical research communications _gvol. 213 _gno. 1 _gp. 367 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1006/bbrc.1995.2139 _zAvailable from publisher's website |
| 999 |
_c7639188 _d7639188 |
||