Items where Author is "Altmüller, J."

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Article

Ghosh, S. G. and Becker, K. and Huang, H. and Dixon-Salazar, T. and Chai, G. and Salpietro, V. and Al-Gazali, L. and Waisfisz, Q. and Wang, H. and Vaux, K. K. and Stanley, V. and Manole, A. and Akpulat, U. and Weiss, M. M. and Efthymiou, S. and Hanna, M. G. and Minetti, C. and Striano, P. and Pisciotta, L. and De Grandis, E. and Altmüller, J. and Nürnberg, P. and Thiele, H. and Yis, U. and Okur, T. D. and Polat, A. I. and Amiri, N. and Doosti, M. and Karimani, E. G. and Toosi, M. B. and Haddad, G. and Karakaya, M. and Wirth, B. and van Hagen, J. M. and Wolf, N. I. and Maroofian, R. and Houlden, H. and Cirak, S. and Gleeson, J. G. (2018) Biallelic Mutations in ADPRHL2, Encoding ADP-Ribosylhydrolase 3, Lead to a Degenerative Pediatric Stress-Induced Epileptic Ataxia Syndrome. American Journal of Human Genetics, 103 (3). pp. 431-439.

This list was generated on Thu Sep 17 20:29:41 2020 EDT.