000 | 01890 a2200589 4500 | ||
---|---|---|---|
005 | 20250516042239.0 | ||
264 | 0 | _c20120118 | |
008 | 201201s 0 0 eng d | ||
022 | _a1432-1203 | ||
024 | 7 |
_a10.1007/s00439-011-1018-5 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aRehman, Atteeq U | |
245 | 0 | 0 |
_aMutations of GIPC3 cause nonsyndromic hearing loss DFNB72 but not DFNB81 that also maps to chromosome 19p. _h[electronic resource] |
260 |
_bHuman genetics _cDec 2011 |
||
300 |
_a759-65 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdaptor Proteins, Signal Transducing |
650 | 0 | 4 | _aAmino Acid Sequence |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 |
_aCarrier Proteins _xgenetics |
650 | 0 | 4 | _aChromosomes, Human, Pair 19 |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aFrameshift Mutation |
650 | 0 | 4 |
_aGenes, Recessive _xgenetics |
650 | 0 | 4 | _aGenetic Linkage |
650 | 0 | 4 | _aGenetic Loci |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 |
_aHearing Loss _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aPedigree |
700 | 1 | _aGul, Khitab | |
700 | 1 | _aMorell, Robert J | |
700 | 1 | _aLee, Kwanghyuk | |
700 | 1 | _aAhmed, Zubair M | |
700 | 1 | _aRiazuddin, Saima | |
700 | 1 | _aAli, Rana A | |
700 | 1 | _aShahzad, Mohsin | |
700 | 1 | _aJaleel, Ateeq-Ul | |
700 | 1 | _aAndrade, Paula B | |
700 | 1 | _aKhan, Shaheen N | |
700 | 1 | _aKhan, Saadullah | |
700 | 1 | _aBrewer, Carmen C | |
700 | 1 | _aAhmad, Wasim | |
700 | 1 | _aLeal, Suzanne M | |
700 | 1 | _aRiazuddin, Sheikh | |
700 | 1 | _aFriedman, Thomas B | |
773 | 0 |
_tHuman genetics _gvol. 130 _gno. 6 _gp. 759-65 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00439-011-1018-5 _zAvailable from publisher's website |
999 |
_c20916571 _d20916571 |