000			02012 a2200649 4500
005			20250513183039.0
264		0	_c19990708
008			199907s 0 0 eng d
022			_a0964-6906
024	7		_a10.1093/hmg/8.6.971 _2doi
040			_aNLM _beng _cNLM
100	1		_aRickman, L
245	0	0	_aN-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratoderma. _h[electronic resource]
260			_bHuman molecular genetics _cJun 1999
300			_a971-6 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAmino Acid Sequence
650	0	4	_aBase Sequence
650	0	4	_aCadherins _xgenetics
650	0	4	_aCytoskeletal Proteins _xgenetics
650	0	4	_aDNA _xchemistry
650	0	4	_aDNA Mutational Analysis
650	0	4	_aDesmoglein 1
650	0	4	_aDesmogleins
650	0	4	_aDesmoplakins
650	0	4	_aDesmosomes _xchemistry
650	0	4	_aExons _xgenetics
650	0	4	_aFamily Health
650	0	4	_aFemale
650	0	4	_aFoot Dermatoses _xgenetics
650	0	4	_aGenes, Dominant
650	0	4	_aGenetic Linkage
650	0	4	_aHumans
650	0	4	_aKeratoderma, Palmoplantar _xgenetics
650	0	4	_aMale
650	0	4	_aMolecular Sequence Data
650	0	4	_aPedigree
650	0	4	_aPoint Mutation
650	0	4	_aPolymorphism, Single-Stranded Conformational
650	0	4	_aRNA Splicing _xgenetics
650	0	4	_aRNA, Messenger _xgenetics
650	0	4	_aSequence Deletion
650	0	4	_aSkin _xmetabolism
700	1		_aSimrak, D
700	1		_aStevens, H P
700	1		_aHunt, D M
700	1		_aKing, I A
700	1		_aBryant, S P
700	1		_aEady, R A
700	1		_aLeigh, I M
700	1		_aArnemann, J
700	1		_aMagee, A I
700	1		_aKelsell, D P
700	1		_aBuxton, R S
773	0		_tHuman molecular genetics _gvol. 8 _gno. 6 _gp. 971-6
856	4	0	_uhttps://doi.org/10.1093/hmg/8.6.971 _zAvailable from publisher's website
999			_c10290854 _d10290854