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Pubmed ID :19262603
Publication Date : //

ABCA12 is a major causative gene for non-bullous congenital ichthyosiform erythroderma.



Authors : Sakai Kaori , Akiyama Masashi , Yanagi Teruki , McMillan James R , Suzuki Tamio , Tsukamoto Katsuhiko , Sugiyama Hideaki , Hatano Yuji , Hayashitani Michiko , Takamori Kenji , Nakashima Keiko , Shimizu Hiroshi ,

Related products :

Catalog number Product name Quantity
ICR4 ICR1 Gene ichthyosis congenita I, erythromatous lamellar ichthyosis, ichthyosiform erythroderma
EIAAB12225 230 kDa bullous pemphigoid antigen,230_240 kDa bullous pemphigoid antigen,BP230,BP240,BPA,BPAG1,Bullous pemphigoid antigen,Bullous pemphigoid antigen 1,DMH,DST,DT,Dystonia musculorum protein,Dystonin,
28-975 HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expr 0.1 mg
25-292 HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expr 0.05 mg
29-327 HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expr 0.1 mg
28-976 HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expr 0.1 mg
ABCA12 ABCA1 Gene ATP-binding cassette, sub-family A (ABC1), member 1
ABCA2 ABCA12 Gene ATP-binding cassette, sub-family A (ABC1), member 12
CCT3 CCT Gene cataract, congenital, total
CD101 CCV Gene cataract, congenital, Volkmann type
HTGH HTC1 Gene hypertrichosis 1 (universalis, congenital)
GLCE GLC3C Gene glaucoma 3, primary congenital, C
LCE1A LCA9 Gene Leber congenital amaurosis 9
LCAT LCA5L Gene Leber congenital amaurosis 5-like
HTGS HTC2 Gene hypertrichosis 2 (generalized, congenital)
LCA9 LCA5 Gene Leber congenital amaurosis 5
NYX NYS4 Gene nystagmus 4, congenital autosomal dominant
NYS4 NYS2 Gene nystagmus 2, congenital autosomal dominant
NYS5 NYS3 Gene nystagmus 3, congenital autosomal dominant
CDB2 CDAN1 Gene congenital dyserythropoietic anemia, type I
DFN6 DFN4 Gene deafness, X-linked 4, congenital sensorineural
BSG BSCL2 Gene Berardinelli-Seip congenital lipodystrophy 2 (seipin)
DFN5 DFN2 Gene deafness, X-linked 2, perceptive, congenital
FER1L5 FEOM3 Gene fibrosis of extraocular muscles, congenital, 3
CDC123 CDAN3 Gene congenital dyserythropoietic anemia, type III


 

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