000 01533 a2200457 4500
005 20250513143009.0
264 0 _c19980720
008 199807s 0 0 ger d
022 _a0023-2165
024 7 _a10.1055/s-2008-1034852
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMeins, M
245 0 0 _a[Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family].
_h[electronic resource]
260 _bKlinische Monatsblatter fur Augenheilkunde
_cMar 1998
300 _a154-8 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChromosome Aberrations
_xgenetics
650 0 4 _aChromosome Disorders
650 0 4 _aChromosomes, Human, Pair 5
650 0 4 _aCorneal Dystrophies, Hereditary
_xclassification
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDNA, Complementary
_xgenetics
650 0 4 _aExtracellular Matrix Proteins
_xgenetics
650 0 4 _aEye Proteins
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
_xgenetics
650 0 4 _aGenetic Carrier Screening
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aPedigree
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aRNA, Messenger
_xgenetics
700 1 _aKohlhaas, M
700 1 _aRichard, G
700 1 _aGal, A
773 0 _tKlinische Monatsblatter fur Augenheilkunde
_gvol. 212
_gno. 3
_gp. 154-8
856 4 0 _uhttps://doi.org/10.1055/s-2008-1034852
_zAvailable from publisher's website
999 _c9559499
_d9559499