المؤلفون: Johal S.C., Amato A.A., Demmer L.A., Jonas J., Darras B.T., Bird T.D., Laurino M., Welt S.I., Trotter C., Guicheney P., Das S., Mandel J.-L., Beggs A.H., Biancalana V., Laporte J., Jern C., Erby L.A.H., Smith S.A., Roggenbuck J., Crowe C.A., Spitale A.B., Böhm J., DeChene E.T., Bitoun M., Pierson C.R., Schaefer E., Karasoy H., Dempsey M.A., Klein F., Dondaine N., Kretz C., Haumesser N., Poirson C., Toussaint A., Greenleaf R.S., Barger M.A., Mahoney L.J., Kang P.B., Zanoteli E., Vissing J., Witting N., Echaniz-Laguna A., Wallgren-Pettersson C., Dowling J., Merlini L., Oldfors A., Ousager L.B., Melki J., Krause A., Oliveira A.S.B., Petit F., Jacquette A., Chaussenot A., Mowat D., Leheup B., Cristofano M., Aldea J.J.P., Michel F., Furby A., Llona J.E.B., Van Coster R., Bertini E., Urtizberea J.A., Drouin-Garraud V., roud C.B., Prudhon B., Bedford M., Mathews K.

مصطلحات موضوعية: BIN1, ADCNM, Centronuclear myopathy, Charcot-marie-tooth neuropathy, CMT2M, CMTD1B, Congenital myopathy, Di-CMTB, DNM2, Endocytosis, Hereditary motor and sensory neuropathy type II, HMSNII, MTM1, Myotubular myopathy, RYR1

العلاقة: Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Human Mutation; https://hdl.handle.net/11454/18725Test; https://doi.org/10.1002/humu.22067Test; 33; 949; 959

الإتاحة: https://doi.org/10.1002/humu.22067Test
https://hdl.handle.net/11454/18725Test

المؤلفون: Böhm J., Biancalana V., DeChene E.T., Bitoun M., Pierson C.R., Schaefer E., Karasoy H., Dempsey M.A., Klein F., Dondaine N., Kretz C., Haumesser N., Poirson C., Toussaint A., Greenleaf R.S., Barger M.A., Mahoney L.J., Kang P.B., Zanoteli E., Vissing J., Witting N., Echaniz-Laguna A., Wallgren-Pettersson C., Dowling J., Merlini L., Oldfors A., Ousager L.B., Melki J., Krause A., Jern C., Oliveira A.S.B., Petit F., Jacquette A., Chaussenot A., Mowat D., Leheup B., Cristofano M., Aldea J.J.P., Michel F., Furby A., Llona J.E.B., Van Coster R., Bertini E., Urtizberea J.A., Drouin-Garraud V., roud C.B., Prudhon B., Bedford M., Mathews K., Erby L.A.H., Smith S.A., Roggenbuck J., Crowe C.A., Spitale A.B., Johal S.C., Amato A.A., Demmer L.A., Jonas J., Darras B.T., Bird T.D., Laurino M., Welt S.I., Trotter C., Guicheney P., Das S., Mandel J.-L., Beggs A.H., Laporte J.

المساهمون: Ege Üniversitesi

مصطلحات موضوعية: ADCNM, BIN1, Centronuclear myopathy, Charcot-marie-tooth neuropathy, CMT2M, CMTD1B, Congenital myopathy, Di-CMTB, DNM2, Endocytosis, Hereditary motor and sensory neuropathy type II, HMSNII, MTM1, Myotubular myopathy, RYR1

العلاقة: Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; Human Mutation; https://doi.org/10.1002/humu.22067Test; https://hdl.handle.net/11454/18725Test; 33; 949; 959

الإتاحة: https://doi.org/10.1002/humu.22067Test
https://hdl.handle.net/11454/18725Test