000			01472 a2200433 4500
005			20250514190315.0
264		0	_c20040824
008			200408s 0 0 eng d
022			_a0378-1119
024	7		_a10.1016/j.gene.2004.02.037 _2doi
040			_aNLM _beng _cNLM
100	1		_aBriscoe, Adriana D
245	0	0	_aThe spectrum of human rhodopsin disease mutations through the lens of interspecific variation. _h[electronic resource]
260			_bGene _cMay 2004
300			_a107-18 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAmino Acid Sequence
650	0	4	_aAmino Acid Substitution
650	0	4	_aAnimals
650	0	4	_aCodon _xgenetics
650	0	4	_aConserved Sequence _xgenetics
650	0	4	_aEvolution, Molecular
650	0	4	_aGene Frequency
650	0	4	_aGenetic Variation
650	0	4	_aGenotype
650	0	4	_aHumans
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutation
650	0	4	_aPhenotype
650	0	4	_aPhylogeny
650	0	4	_aRetinal Diseases _xgenetics
650	0	4	_aRetinitis Pigmentosa _xgenetics
650	0	4	_aRhodopsin _xgenetics
650	0	4	_aSpecies Specificity
700	1		_aGaur, Charu
700	1		_aKumar, Sudhir
773	0		_tGene _gvol. 332 _gp. 107-18
856	4	0	_uhttps://doi.org/10.1016/j.gene.2004.02.037 _zAvailable from publisher's website
999			_c14854102 _d14854102