Search Results - "Street, V.A."

Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes by Street, V.A., Meekins, G., Lipe, H.P., Seltzer, W.K., Carter, G.T., Kraft, G.H., Bird, T.D.

“…Charcot–Marie–Tooth Hereditary Neuropathy is a heterogeneous syndrome associated with mutations in several different genes including peripheral myelin protein…”
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Voltage-gated potassium channel genes are clustered in paralogous regions of the mouse genome by Lock, L F, Gilbert, D J, Street, V A, Migeon, M B, Jenkins, N A, Copeland, N G, Tempel, B L

“…Cloning of the Drosophila Shaker gene established that a neurological phenotype including locomotor dysfunction can be caused by a mutation in a voltage-gated…”
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Molecular genetic analysis of distal mouse chromosome 6 defines gene order and positions of the deafwaddler and opisthotonos mutations by STREET, V. A, ROBINSON, L. C, ERFORD, S. K, TEMPEL, B. L

“…Two neurological mutants deafwaddler (dfw) and opisthotonos (opt) and a cluster of three Shaker-like potassium (K) channel genes Kcna1, Kcna5, and Kcna6 were…”
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