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