Bedoyan, J.K., Schaibley, V.M., Peng, W., Bai, Y., Mondal, K., Shetty, A.C., Durham, M., Micucci, J.A., Dhiraaj, A., Skidmore, J.M., Kaplan, J.B., Skinner, C., Schwartz, C.E., Antonellis, A., Zwick, M.E., Cavalcoli, J.D., Li, J.Z., and Martin, D.M. (2012) Disruption of RAB40AL function leads to Martin-Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. Journal of Medical Genetics. 49(5):332-340

Son, W., Jeong, H.S., Nam, D.E., Lee, A.J., Nam, S.H., Lee, J.E., Choi, B.O., Chung, K.W. (2023) Peripheral Neuropathy and Decreased Locomotion of a RAB40B Mutation in Human and Model Animals. Experimental Neurobiology. 32:410422410-422

van der Sar, A.M., Spaink, H.P., Zakrzewska, A., Bitter, W., and Meijer, A.H. (2009) Specificity of the zebrafish host transcriptome response to acute and chronic mycobacterial infection and the role of innate and adaptive immune components. Molecular immunology. 46(11-12):2317-2332

Son, W., Jeong, H.S., Nam, D.E., Lee, A.J., Nam, S.H., Lee, J.E., Choi, B.O., Chung, K.W. (2023) Peripheral Neuropathy and Decreased Locomotion of a RAB40B Mutation in Human and Model Animals. Experimental Neurobiology. 32:410422410-422

Bedoyan, J.K., Schaibley, V.M., Peng, W., Bai, Y., Mondal, K., Shetty, A.C., Durham, M., Micucci, J.A., Dhiraaj, A., Skidmore, J.M., Kaplan, J.B., Skinner, C., Schwartz, C.E., Antonellis, A., Zwick, M.E., Cavalcoli, J.D., Li, J.Z., and Martin, D.M. (2012) Disruption of RAB40AL function leads to Martin-Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. Journal of Medical Genetics. 49(5):332-340

Strausberg,R.L., Feingold,E.A., Grouse,L.H., Derge,J.G., Klausner,R.D., Collins,F.S., Wagner,L., Shenmen,C.M., Schuler,G.D., Altschul,S.F., Zeeberg,B., Buetow,K.H., Schaefer,C.F., Bhat,N.K., Hopkins,R.F., Jordan,H., Moore,T., Max,S.I., Wang,J., Hsieh,F., Diatchenko,L., Marusina,K., Farmer,A.A., Rubin,G.M., Hong,L., Stapleton,M., Soares,M.B., Bonaldo,M.F., Casavant,T.L., Scheetz,T.E., Brownstein,M.J., Usdin,T.B., Toshiyuki,S., Carninci,P., Prange,C., Raha,S.S., Loquellano,N.A., Peters,G.J., Abramson,R.D., Mullahy,S.J., Bosak,S.A., McEwan,P.J., McKernan,K.J., Malek,J.A., Gunaratne,P.H., Richards,S., Worley,K.C., Hale,S., Garcia,A.M., Gay,L.J., Hulyk,S.W., Villalon,D.K., Muzny,D.M., Sodergren,E.J., Lu,X., Gibbs,R.A., Fahey,J., Helton,E., Ketteman,M., Madan,A., Rodrigues,S., Sanchez,A., Whiting,M., Madan,A., Young,A.C., Shevchenko,Y., Bouffard,G.G., Blakesley,R.W., Touchman,J.W., Green,E.D., Dickson,M.C., Rodriguez,A.C., Grimwood,J., Schmutz,J., Myers,R.M., Butterfield,Y.S., Krzywinski,M.I., Skalska,U., Smailus,D.E., Schnerch,A., Schein,J.E., Jones,S.J., and Marra,M.A. (2002) Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proceedings of the National Academy of Sciences of the United States of America. 99(26):16899-903