| 000 | 01444 a2200409 4500 | ||
|---|---|---|---|
| 005 | 20250513003734.0 | ||
| 264 | 0 | _c19810723 | |
| 008 | 198107s 0 0 eng d | ||
| 022 | _a0148-639X | ||
| 024 | 7 |
_a10.1002/mus.880040107 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aKark, R A | |
| 245 | 0 | 0 |
_aMultiple genotypes, multiple phenotypes, and partial defects. _h[electronic resource] |
| 260 |
_bMuscle & nerve _c |
||
| 300 |
_a31-40 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review | ||
| 650 | 0 | 4 |
_aAnemia, Hemolytic, Congenital _xgenetics |
| 650 | 0 | 4 |
_aArylsulfatases _xdeficiency |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Variation |
| 650 | 0 | 4 | _aGenotype |
| 650 | 0 | 4 |
_aGlucosephosphate Dehydrogenase Deficiency _xgenetics |
| 650 | 0 | 4 |
_aGlycogen Storage Disease Type V _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aHyperlipoproteinemia Type II _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aModels, Genetic |
| 650 | 0 | 4 |
_aMuscular Atrophy _xgenetics |
| 650 | 0 | 4 |
_aNeuromuscular Diseases _xgenetics |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 |
_aPorphyrias _xgenetics |
| 650 | 0 | 4 |
_aPyruvate Kinase _xdeficiency |
| 650 | 0 | 4 |
_aTay-Sachs Disease _xgenetics |
| 700 | 1 | _aBecker, D M | |
| 773 | 0 |
_tMuscle & nerve _gvol. 4 _gno. 1 _gp. 31-40 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1002/mus.880040107 _zAvailable from publisher's website |
| 999 |
_c7014787 _d7014787 |
||