ADTB3AAmyotrophic lateral sclerosis slow progressing ALS8Amyotrophic lateral sclerosisARC syndromeARL6Bardet Biedl syndromebeta Actinbeta3 spectrinBiomembranes (Traffic)CEDNIK syndromeCell polarityCell secretion (Intracellular transport)Charcot Marie Tooth disease type 2aCharcot Marie Tooth disease type 2bCharcot Marie Tooth diseaseChediak Higashi syndromeChoroideremiaCOG7Congenital disorder of glycosylation type IIeCOPICOPiiCranio lenticulo sutural dysplasiaDeafness (Inherited)
Developmental malformations deafness dystonia OMIM_607371DTNBP1DysferlinElajalde syndrome Griscelli syndrome IIEndoplasmic reticulum (BASKET)EndosomFactor V (Coagulation)Factor VIII (Coagulation)Familial hemophagoctic lymphohistiocytosisGriscelli s syndrome IIIGriscelli s syndrome2Hereditary spastic paraplegia SPG10Hereditary spastic paraplegia SPG4Hermansky Pudlak syndromeHPS1HPS3HPS4HPS5HPS6KIF1BKIF5AKinesinLimb girdle muscular dystrophy type 2B
LMAN1 ERGIC53Lowe s syndromeLYST CHS1Martsolf syndromeMCFD2MiltonMiroMiyoshi s myopathyMLPHMyosin Ia Myo1aMyosin VMyosin Va Myo5aMyosin VIMyosin VIIaMyosin XVa Myo15aNanomedicineOCRL1OMIM_300104Origin of lifePIKfyveRABRAB27ARAB3GAP
RAB7RABGDIAREP1Sar1SEC23ASignal transductionSNAP29SPG20 SpartinSPG4 SpastinSpinal muscular atrophy late onsetSpinocerebellar ataxia5Syntaxin11Troyer syndrome SPG20UNC13D Munc13 4 HPLH3Usher syndrome type IbVAPBVPS33BWarburg Micro syndromeX linked non specific mental retardation
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