000 | 01444 a2200457 4500 | ||
---|---|---|---|
005 | 20250518054914.0 | ||
264 | 0 | _c20200831 | |
008 | 202008s 0 0 eng d | ||
022 | _a1399-0004 | ||
024 | 7 |
_a10.1111/cge.13631 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aBeaman, Glenda M | |
245 | 0 | 0 |
_aA homozygous missense variant in CHRM3 associated with familial urinary bladder disease. _h[electronic resource] |
260 |
_bClinical genetics _c12 2019 |
||
300 |
_a515-520 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aFamily |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHomozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMalaysia |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMutation, Missense _xgenetics |
650 | 0 | 4 |
_aReceptor, Muscarinic M3 _xgenetics |
650 | 0 | 4 |
_aUrinary Bladder Diseases _xgenetics |
700 | 1 | _aGalatà , Gabriella | |
700 | 1 | _aTeik, Keng W | |
700 | 1 | _aUrquhart, Jill E | |
700 | 1 | _aAishah, Ali | |
700 | 1 | _aO'Sullivan, James | |
700 | 1 | _aBhaskar, Sanjeev S | |
700 | 1 | _aWood, Katherine A | |
700 | 1 | _aThomas, Huw B | |
700 | 1 | _aO'Keefe, Raymond T | |
700 | 1 | _aWoolf, Adrian S | |
700 | 1 | _aStuart, Helen M | |
700 | 1 | _aNewman, William G | |
773 | 0 |
_tClinical genetics _gvol. 96 _gno. 6 _gp. 515-520 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1111/cge.13631 _zAvailable from publisher's website |
999 |
_c30033310 _d30033310 |