000 | 01744 a2200541 4500 | ||
---|---|---|---|
005 | 20250514020327.0 | ||
264 | 0 | _c20020409 | |
008 | 200204s 0 0 eng d | ||
022 | _a0890-8508 | ||
024 | 7 |
_a10.1006/mcpr.2001.0371 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aGanesh, S | |
245 | 0 | 0 |
_aMutation screening for Japanese Lafora's disease patients: identification of novel sequence variants in the coding and upstream regulatory regions of EPM2A gene. _h[electronic resource] |
260 |
_bMolecular and cellular probes _cOct 2001 |
||
300 |
_a281-9 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAnimals |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aContig Mapping |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aIn Situ Hybridization, Fluorescence |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 | _aJapan |
650 | 0 | 4 |
_aLafora Disease _xgenetics |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aPolymorphism, Genetic |
650 | 0 | 4 |
_aProtein Tyrosine Phosphatases _xgenetics |
650 | 0 | 4 | _aProtein Tyrosine Phosphatases, Non-Receptor |
650 | 0 | 4 |
_aRegulatory Sequences, Nucleic Acid _xgenetics |
700 | 1 | _aShoda, K | |
700 | 1 | _aAmano, K | |
700 | 1 | _aUchiyama, A | |
700 | 1 | _aKumada, S | |
700 | 1 | _aMoriyama, N | |
700 | 1 | _aHirose, S | |
700 | 1 | _aYamakawa, K | |
773 | 0 |
_tMolecular and cellular probes _gvol. 15 _gno. 5 _gp. 281-9 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1006/mcpr.2001.0371 _zAvailable from publisher's website |
999 |
_c11648828 _d11648828 |