ADAR2ADTB3AALS2 AlsinAlzheimer s diseaseAmyotrophic lateral sclerosis slow progressing ALS8Amyotrophic lateral sclerosisAngiogeninARC syndromeARL6Bardet Biedl syndromebeta Actinbeta3 spectrinCEDNIK syndromeCell secretion (Intracellular transport)Changes in terminologyCharcot Marie Tooth disease type 2aCharcot Marie Tooth disease type 2bChediak Higashi syndromeChoroideremiaCNS (Astrocyte)COG7Congenital disorder of glycosylation type IIeCranio lenticulo sutural dysplasiaCYFIP2Deafness (Inherited)
Developmental malformations deafness dystonia OMIM_607371DTNBP1DysferlinElajalde syndrome Griscelli syndrome IIEpilepsy (Excitotoxicity)ERS UFR (Diseases)Factor V (Coagulation)Factor VIII (Coagulation)Familial hemophagoctic lymphohistiocytosisFrontotemporal lobar degenerationFUS TLSGluR2Griscelli s syndrome IIIGriscelli s syndrome2GSK3Guam Parkinson dementia complexHereditary spastic paraplegia SPG10Hereditary spastic paraplegia SPG4Hermansky Pudlak syndromeHPS1HPS3HPS4HPS5HPS6KIF1B
KIF5ALimb girdle muscular dystrophy type 2BLMAN1 ERGIC53Lowe s syndromeLYST CHS1Martsolf syndromeMCFD2Mitochondria (BASKET)Mitochondria (Dysfunction)Mitochondria (Permeability transition)Miyoshi s myopathyMLPHMyosin Ia Myo1aMyosin Va Myo5aMyosin VIMyosin VIIaMyosin XVa Myo15aOCRL1OMIM_300104Protein (ptm S nitrosylation)Protein disulfide isomeraseRAB27ARAB3GAPRAB7RABGDIA
REP1RNA (Binding proteins)RNA (Editing)SEC23ASelenSNAP29SPG20 SpartinSPG4 SpastinSpinal muscular atrophy late onsetSpinocerebellar ataxia5Superoxide dismutase SODSyntaxin11TDP43Threohydroxyaspartatetrans 1 2 bis mercaptoacetamido cyclohexane ttPDI mimicTroyer syndrome SPG20UNC13D Munc13 4 HPLH3Usher syndrome type IbVAPBVPS33BWarburg Micro syndrome
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