Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model.

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model.

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Many neurological conditions are caused by immensely heterogeneous gene mutations. The diagnostic process is often long and complex with most patients undergoing multiple invasive and costly investigations without ever reaching a conclusive molecular diagnosis. The advent of massively parallel, next...

Bibliografiset tiedot
Päätekijät:	Németh, A, Kwasniewska, A, Lise, S, Parolin Schnekenberg, R, Becker, E, Bera, K, Shanks, M, Gregory, L, Buck, D, Zameel Cader, M, Talbot, K, de Silva, R, Fletcher, N, Hastings, R, Jayawant, S, Morrison, P, Worth, P, Taylor, M, Tolmie, J, O'Regan, M, Valentine, R, Packham, E, Evans, J, Seller, A, Ragoussis, J
Aineistotyyppi:	Journal article
Kieli:	English
Julkaistu:	2013

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