000			01855 a2200577 4500
005			20250516114633.0
264		0	_c20130322
008			201303s 0 0 eng d
022			_a1553-7404
024	7		_a10.1371/journal.pgen.1003001 _2doi
040			_aNLM _beng _cNLM
100	1		_aMahajan, Vinit B
245	0	0	_aCalpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration. _h[electronic resource]
260			_bPLoS genetics _c2012
300			_ae1003001 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650	0	4	_aAmino Acid Sequence
650	0	4	_aBase Sequence
650	0	4	_aCalpain _xchemistry
650	0	4	_aCell Line
650	0	4	_aCells, Cultured
650	0	4	_aChoroid Diseases _xgenetics
650	0	4	_aExome
650	0	4	_aExons
650	0	4	_aEye Diseases, Hereditary _xgenetics
650	0	4	_aFemale
650	0	4	_aGene Expression
650	0	4	_aGenetic Linkage
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aModels, Molecular
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutation
650	0	4	_aPedigree
650	0	4	_aPhenotype
650	0	4	_aPhotoreceptor Cells, Vertebrate _xmetabolism
650	0	4	_aProtein Conformation
650	0	4	_aProtein Transport
650	0	4	_aRetinal Degeneration _xgenetics
650	0	4	_aSequence Alignment
700	1		_aSkeie, Jessica M
700	1		_aBassuk, Alexander G
700	1		_aFingert, John H
700	1		_aBraun, Terry A
700	1		_aDaggett, Heather T
700	1		_aFolk, James C
700	1		_aSheffield, Val C
700	1		_aStone, Edwin M
773	0		_tPLoS genetics _gvol. 8 _gno. 10 _gp. e1003001
856	4	0	_uhttps://doi.org/10.1371/journal.pgen.1003001 _zAvailable from publisher's website
999			_c22175871 _d22175871