| 000 | 01797 a2200541 4500 | ||
|---|---|---|---|
| 005 | 20250514020423.0 | ||
| 264 | 0 | _c20020318 | |
| 008 | 200203s 0 0 eng d | ||
| 022 | _a0960-8966 | ||
| 024 | 7 |
_a10.1016/s0960-8966(01)00252-8 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aDonner, Kati | |
| 245 | 0 | 0 |
_aMutations in the beta-tropomyosin (TPM2) gene--a rare cause of nemaline myopathy. _h[electronic resource] |
| 260 |
_bNeuromuscular disorders : NMD _cFeb 2002 |
||
| 300 |
_a151-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAmino Acid Sequence |
| 650 | 0 | 4 | _aAnimals |
| 650 | 0 | 4 | _aBiopsy |
| 650 | 0 | 4 | _aDNA Primers |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenetic Linkage |
| 650 | 0 | 4 | _aGenetic Markers |
| 650 | 0 | 4 |
_aHaplotypes _xgenetics |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMolecular Sequence Data |
| 650 | 0 | 4 |
_aMuscle, Skeletal _xpathology |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 | _aMutation, Missense |
| 650 | 0 | 4 |
_aMyopathies, Nemaline _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPolymorphism, Single-Stranded Conformational |
| 650 | 0 | 4 | _aProtein Conformation |
| 650 | 0 | 4 | _aReverse Transcriptase Polymerase Chain Reaction |
| 650 | 0 | 4 | _aSequence Alignment |
| 650 | 0 | 4 | _aSequence Homology, Amino Acid |
| 650 | 0 | 4 |
_aTropomyosin _xchemistry |
| 700 | 1 | _aOllikainen, Miina | |
| 700 | 1 | _aRidanpää, Maaret | |
| 700 | 1 | _aChristen, Hans-Jürgen | |
| 700 | 1 | _aGoebel, Hans H | |
| 700 | 1 | _ade Visser, Marianne | |
| 700 | 1 | _aPelin, Katarina | |
| 700 | 1 | _aWallgren-Pettersson, Carina | |
| 773 | 0 |
_tNeuromuscular disorders : NMD _gvol. 12 _gno. 2 _gp. 151-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0960-8966(01)00252-8 _zAvailable from publisher's website |
| 999 |
_c11651764 _d11651764 |
||