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Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Sequence Deletion (genetics) »
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Sequence Deletion < Sequence Deletion (genetics) < Sequence Homology, Amino Acid  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 6.
Ident.Authors (with country if any)Title
002251 (2008) Michelangelo Mancuso ; Daniele Orsucci ; Sara Gori ; Roberto Ceravolo ; Gabriele SicilianoMitochondrial DNA single deletion in a patient with postural tremor.
002F43 (2011) Arpan R. Mehta [Canada] ; Susan H. Fox ; Mark Tarnopolsky ; Grace YoonMitochondrial mimicry of multiple system atrophy of the cerebellar subtype.
003005 (2011) Valentina Garibotto [Italie] ; Luigi M. Romito ; Antonio E. Elia ; Paola Soliveri ; Andrea Panzacchi ; Assunta Carpinelli ; Michele Tinazzi ; Alberto Albanese ; Daniela PeraniIn vivo evidence for GABA(A) receptor changes in the sensorimotor system in primary dystonia.
003098 (2011) Aida Ormazabal ; Mercedes Serrano ; Angels Garcia-Cazorla ; Jaume Campistol ; Rafael Artuch ; Pedro Castro De Castro ; Estíbaliz Barredo-Valderrama ; Judith Armstrong ; Claudio Toma ; Bru CormandDeletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.
003155 (2011) Sharon Hassin-Baer [Israël] ; Nobutaka Hattori ; Oren S. Cohen ; Magdalena Massarwa ; Simon D. Israeli-Korn ; Rivka InzelbergPhenotype of the 202 adenine deletion in the parkin gene: 40 years of follow-up.
003816 (2012) Jessie Theuns [Belgique] ; David Crosiers ; Luc Debaene ; Karen Nuytemans ; Bram Meeus ; Kristel Sleegers ; Dirk Goossens ; Ellen Corsmit ; Ellen Elinck ; Karin Peeters ; Maria Mattheijssens ; Barbara Pickut ; Jurgen Del-Favero ; Sebastiaan Engelborghs ; Peter Paul De Deyn ; Patrick Cras ; Christine Van BroeckhovenGuanosine triphosphate cyclohydrolase 1 promoter deletion causes dopa-responsive dystonia.

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   |clé=    Sequence Deletion (genetics)
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