000 01411 a2200433 4500
005 20250517231354.0
264 0 _c20190410
008 201904s 0 0 eng d
022 _a1744-5094
024 7 _a10.1080/13816810.2018.1502792
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aLenk, Janine
245 0 0 _aPosterior amorphous corneal dystrophy in a patient with 12q21.33 deletion.
_h[electronic resource]
260 _bOphthalmic genetics
_c10 2018
300 _a645-647 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aChild
650 0 4 _aChromosome Deletion
650 0 4 _aChromosomes, Human, Pair 12
650 0 4 _aCorneal Dystrophies, Hereditary
_xgenetics
650 0 4 _aDecorin
_xgenetics
650 0 4 _aHaploinsufficiency
650 0 4 _aHumans
650 0 4 _aLumican
_xgenetics
650 0 4 _aMale
650 0 4 _aPrognosis
650 0 4 _aProteoglycans
_xgenetics
650 0 4 _aSmall Leucine-Rich Proteoglycans
_xgenetics
700 1 _aPorrmann, Joseph
700 1 _aSmitka, Martin
700 1 _aEger, Ines
700 1 _aSchröck, Evelin
700 1 _aHackmann, Karl
700 1 _aHerber, Robert
700 1 _aRaiskup, Frederik
700 1 _aTzschach, Andreas
773 0 _tOphthalmic genetics
_gvol. 39
_gno. 5
_gp. 645-647
856 4 0 _uhttps://doi.org/10.1080/13816810.2018.1502792
_zAvailable from publisher's website
999 _c28682180
_d28682180