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Results: 1-3 |
Results: 3
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
Authors: Eunson, LH Rea, R Zuberi, SM Youroukos, S Panayiotopoulos, CP Liguori, R Avoni, P McWilliam, RC Stephenson, JBP Hanna, MG Kullmann, DM Spauschus, A
Citation: Lh. Eunson et al., Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability, ANN NEUROL, 48(4), 2000, pp. 647-656
Muscle ultrasound in the assessment of suspected neuromuscular disease in childhood
Authors: Zuberi, SM Matta, N Nawaz, S Stephenson, JB McWilliam, RC Hollman, A
Citation: Sm. Zuberi et al., Muscle ultrasound in the assessment of suspected neuromuscular disease in childhood, NEUROMUSC D, 9(4), 1999, pp. 203-207
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1)associates with episodic ataxia type 1 and sometimes with partial epilepsy
Authors: Zuberi, SM Eunson, LH Spauschus, A De Silva, R Tolmie, J Wood, NW McWilliam, RC Stephenson, JPB Kullmann, DM Hanna, MG
Citation: Sm. Zuberi et al., A novel mutation in the human voltage-gated potassium channel gene (Kv1.1)associates with episodic ataxia type 1 and sometimes with partial epilepsy, BRAIN, 122, 1999, pp. 817-825
Risultati: 1-3 |