DOI Ghosh, S.G., Becker, K., Huang, H., Salazar, T.D., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K.K., Stanley, V., Manole, A.,
AKPULAT, U., Weiss, M.M., Efthymiou, S., Hanna, M.G., Minetti, C., Striano, P., Pisciotta, L., Grandis, E.D., Altmuller, J., Weixler, L., Nurnberg, P., Thiele, H., Yis, U., Okur, T.D., Polat, A.I., Amiri, N., Doosti, M., Karimani, E.G., Toosi, M.B., Haddad, G., Karakaya, M., Wirth, B., Hagen, J.M.V., Wolf, N.I., Maroofian, R., Houlden, H., Cirak, S., Gleeson, J.G. (2021) "
Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (vol 103, pg 431, 2018)",
AMERICAN JOURNAL OF HUMAN GENETICS, 108 (12) pp. 2385-2385
DOI " data-bs-content-id="YazarBilgi-34748">
Ghosh, S.G., Becker, K., Huang, H., Salazar, T.D., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K.K., Stanley, V., Manole, A., AKPULAT, U., Weiss, M.M., Efthymiou, S., Hanna, M.G., Minetti, C., Striano, P., Pisciotta, L., Grandis, E.D., Altmuller, J., Weixler, L., Nurnberg, P., Thiele, H., Yis, U., Okur, T.D., Polat, A.I., Amiri, N., Doosti, M., Karimani, E.G., Toosi, M.B., Haddad, G., Karakaya, M., Wirth, B., Hagen, J.M.V., Wolf, N.I., Maroofian, R., Houlden, H., Cirak, S., Gleeson, J.G. (2021) "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (vol 103, pg 431, 2018)", AMERICAN JOURNAL OF HUMAN GENETICS, 108 (12) pp. 2385-2385 DOI Ghosh, S.G., Becker, K., Huang, H., Salazar, T.D., Chai, G., Salpietro, V., Al-Gazali, L., Waisfisz, Q., Wang, H., Vaux, K.K., Stanley, V., Manole, A., AKPULAT, U., Weiss, M.M., Efthymiou, S., Hanna, M.G., Minetti, C., Striano, P., Pisciotta, L., Grandis, E.D., Altmuller, J., Weixler, L., Nurnberg, P., Thiele, H., Yis, U., Okur, T.D., Polat, A.I., Amiri, N., Doosti, M., Karimani, E.G., Toosi, M.B., Haddad, G., Karakaya, M., Wirth, B., Hagen, J.M.V., Wolf, N.I., Maroofian, R., Houlden, H., Cirak, S., Gleeson, J.G. (2021) "Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome (vol 103, pg 431, 2018)", AMERICAN JOURNAL OF HUMAN GENETICS, 108 (12) pp. 2385-2385 DOI
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