000 01702 a2200469 4500
005 20250515011924.0
264 0 _c20060228
008 200602s 0 0 ger d
022 _a0023-2165
024 7 _a10.1055/s-2005-858589
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aGrĂ¼nauer-Kloevekorn, C
245 0 0 _a[Molecular genetic analysis of the BIGH3 gene in lattice type I (Biber-Haab-Dimmer) and granular type II (Avellino) corneal dystrophy: is indirect mutation analysis for hot spots recommended?].
_h[electronic resource]
260 _bKlinische Monatsblatter fur Augenheilkunde
_cDec 2005
300 _a1017-23 p.
_bdigital
500 _aPublication Type: Case Reports; English Abstract; Journal Article
650 0 4 _aAdult
650 0 4 _aCorneal Dystrophies, Hereditary
_xdiagnosis
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDiagnosis, Differential
650 0 4 _aExtracellular Matrix Proteins
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Predisposition to Disease
_xgenetics
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aPhenotype
650 0 4 _aPoint Mutation
650 0 4 _aRisk Assessment
_xmethods
650 0 4 _aRisk Factors
650 0 4 _aTransforming Growth Factor beta
_xgenetics
700 1 _aBräutigam, S
700 1 _aWolter-Roessler, M
700 1 _aTost, F
700 1 _aWeidle, E
700 1 _aFroster, U
700 1 _aDuncker, G I W
773 0 _tKlinische Monatsblatter fur Augenheilkunde
_gvol. 222
_gno. 12
_gp. 1017-23
856 4 0 _uhttps://doi.org/10.1055/s-2005-858589
_zAvailable from publisher's website
999 _c15999230
_d15999230