000			01724 a2200517 4500
005			20250513115854.0
264		0	_c19970515
008			199705s 0 0 eng d
022			_a0964-6906
024	7		_a10.1093/hmg/6.3.425 _2doi
040			_aNLM _beng _cNLM
100	1		_aCecchi, C
245	0	0	_aThe mottled mouse as a model for human Menkes disease: identification of mutations in the Atp7a gene. _h[electronic resource]
260			_bHuman molecular genetics _cMar 1997
300			_a425-33 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdenosine Triphosphatases _xgenetics
650	0	4	_aAnimals
650	0	4	_aCarrier Proteins _xgenetics
650	0	4	_aCation Transport Proteins
650	0	4	_aCopper _xmetabolism
650	0	4	_aCopper-Transporting ATPases
650	0	4	_aDNA Mutational Analysis
650	0	4	_aDNA Primers _xchemistry
650	0	4	_aDisease Models, Animal
650	0	4	_aElectrophoresis, Polyacrylamide Gel
650	0	4	_aEmbryo, Mammalian _xmetabolism
650	0	4	_aFluorescence
650	0	4	_aHeterozygote
650	0	4	_aHumans
650	0	4	_aMenkes Kinky Hair Syndrome _xgenetics
650	0	4	_aMice
650	0	4	_aMutation
650	0	4	_aPhenotype
650	0	4	_aPolymorphism, Genetic
650	0	4	_aRNA, Messenger _xgenetics
650	0	4	_aRecombinant Fusion Proteins
650	0	4	_aSequence Analysis
650	0	4	_aSequence Deletion
650	0	4	_aTranscription, Genetic
700	1		_aBiasotto, M
700	1		_aTosi, M
700	1		_aAvner, P
773	0		_tHuman molecular genetics _gvol. 6 _gno. 3 _gp. 425-33
856	4	0	_uhttps://doi.org/10.1093/hmg/6.3.425 _zAvailable from publisher's website
999			_c9129012 _d9129012