ADTB3AAmphiphysinAmyotrophic lateral sclerosis slow progressing ALS8Amyotrophic lateral sclerosisARC syndromeARL6Bardet Biedl syndromebeta Actinbeta3 spectrinBiomembranes (BASKET)Biomembranes (Repair)CEDNIK syndromeCell secretion (Intracellular transport)Charcot Marie Tooth disease type 2aCharcot Marie Tooth disease type 2bChediak Higashi syndromeChoroideremiaCOG7Congenital disorder of glycosylation type IIeCranio lenticulo sutural dysplasiaDeafness (Inherited)
Developmental malformations deafness dystonia OMIM_607371DTNBP1DysferlinElajalde syndrome Griscelli syndrome IIFactor V (Coagulation)Factor VIII (Coagulation)Familial hemophagoctic lymphohistiocytosisGriscelli s syndrome IIIGriscelli s syndrome2Hereditary spastic paraplegia SPG10Hereditary spastic paraplegia SPG4Hermansky Pudlak syndromeHPS1HPS3HPS4HPS5HPS6JunctophilinKIF1BKIF5ALimb girdle muscular dystrophy type 2B
LMAN1 ERGIC53Lowe s syndromeLYST CHS1Martsolf syndromeMCFD2MitsuguminMiyoshi s myopathyMLPHMuscle (Diseases)Muscle (Physiology)Myopathy (Distal with anterior tibial onset)Myosin Ia Myo1aMyosin Va Myo5aMyosin VIMyosin VIIaMyosin XVa Myo15aMyotubularinOCRL1OMIM_300104RAB27ARAB3GAP
RAB7RABGDIAReceptor (Dihydropyridine)Receptor (Ryanodine)REP1Sarcoplasmic reticulumSEC23ASNAP29SPG20 SpartinSPG4 SpastinSpinal muscular atrophy late onsetSpinocerebellar ataxia5Syntaxin11T tubulusTroyer syndrome SPG20UNC13D Munc13 4 HPLH3Usher syndrome type IbVAPBVPS33BWarburg Micro syndrome
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