000 | 01852 a2200577 4500 | ||
---|---|---|---|
005 | 20250514002134.0 | ||
264 | 0 | _c20010802 | |
008 | 200108s 0 0 eng d | ||
022 | _a0378-1119 | ||
024 | 7 |
_a10.1016/s0378-1119(01)00415-2 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aSeranski, P | |
245 | 0 | 0 |
_aRAI1 is a novel polyglutamine encoding gene that is deleted in Smith-Magenis syndrome patients. _h[electronic resource] |
260 |
_bGene _cMay 2001 |
||
300 |
_a69-76 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAbnormalities, Multiple _xgenetics |
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 | _aBlotting, Northern |
650 | 0 | 4 | _aCell Line |
650 | 0 | 4 | _aChromosome Deletion |
650 | 0 | 4 |
_aChromosomes, Human, Pair 17 _xgenetics |
650 | 0 | 4 |
_aDNA _xchemistry |
650 | 0 | 4 |
_aDNA, Complementary _xchemistry |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGene Deletion |
650 | 0 | 4 | _aGene Expression |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aIntellectual Disability _xpathology |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 |
_aPeptides _xgenetics |
650 | 0 | 4 |
_aProteins _xgenetics |
650 | 0 | 4 |
_aPsychomotor Disorders _xpathology |
650 | 0 | 4 |
_aRNA _xgenetics |
650 | 0 | 4 | _aSequence Analysis, DNA |
650 | 0 | 4 | _aSequence Homology, Amino Acid |
650 | 0 | 4 | _aSyndrome |
650 | 0 | 4 | _aTissue Distribution |
650 | 0 | 4 | _aTrans-Activators |
650 | 0 | 4 | _aTranscription Factors |
650 | 0 | 4 |
_aTrinucleotide Repeats _xgenetics |
700 | 1 | _aHoff, C | |
700 | 1 | _aRadelof, U | |
700 | 1 | _aHennig, S | |
700 | 1 | _aReinhardt, R | |
700 | 1 | _aSchwartz, C E | |
700 | 1 | _aHeiss, N S | |
700 | 1 | _aPoustka, A | |
773 | 0 |
_tGene _gvol. 270 _gno. 1-2 _gp. 69-76 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/s0378-1119(01)00415-2 _zAvailable from publisher's website |
999 |
_c11334402 _d11334402 |