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