| 000 | 00878 a2200241 4500 | ||
|---|---|---|---|
| 005 | 20250517210330.0 | ||
| 264 | 0 | _c20180511 | |
| 008 | 201805s 0 0 eng d | ||
| 022 | _a1469-8749 | ||
| 024 | 7 |
_a10.1111/dmcn.13762 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aSchoser, Benedikt | |
| 245 | 0 | 0 |
_aNovel Pompe disease phenotype: a treatment-related modified phenotype neglecting the brain. _h[electronic resource] |
| 260 |
_bDevelopmental medicine and child neurology _c06 2018 |
||
| 300 |
_a536 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Comment | ||
| 650 | 0 | 4 | _aBrain |
| 650 | 0 | 4 | _aGlycogen Storage Disease Type II |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aPhenotype |
| 773 | 0 |
_tDevelopmental medicine and child neurology _gvol. 60 _gno. 6 _gp. 536 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1111/dmcn.13762 _zAvailable from publisher's website |
| 999 |
_c28236829 _d28236829 |
||