Erratum to: A novel, in-frame KMT2B deletion in a patient with apparently isolated, generalized dystonia (Movement Disorders, (2017), 32, 10, (1495-1497), 10.1002/mds.27137);A novel, in-frame KMT2B deletion in a patient with apparently isolated, generalized dystonia

Movement Disorders

Volumn 32, Issue 10, 2017, Pages 1495-1497

  Lange, Lara M ^a   Tunc, Sinem ^a,b   Tennstedt, Stephanie ^a   Münchau, Alexander ^a,b   Klein, Christine ^a,b   Assmann, Birgit ^c   Lohmann, Katja ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

^b UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^c UNIVERSITY HOSPITAL HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHOLINERGIC RECEPTOR BLOCKING AGENT; LYSINE; LYSINE METHYLTRANSFERASE 2B; METHYLTRANSFERASE; UNCLASSIFIED DRUG; HISTONE LYSINE METHYLTRANSFERASE; KMT2B PROTEIN, HUMAN;

CASE REPORT; CHILD; CLINICAL ARTICLE; FEMALE; GENE DELETION; GENERALIZED DYSTONIA; HUMAN; INFORMED CONSENT; LABORATORY TEST; LETTER; MEDICAL EXAMINATION; MICROCEPHALY; MYOCLONUS; PRIORITY JOURNAL; SCHOOL CHILD; SCOLIOSIS; WHOLE EXOME SEQUENCING; DNA MUTATIONAL ANALYSIS; DYSTONIA; GENETICS;

CHILD; DNA MUTATIONAL ANALYSIS; DYSTONIA; FEMALE; HISTONE-LYSINE N-METHYLTRANSFERASE; HUMANS; SEQUENCE DELETION;

EID: 85031309407     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.27254     Document Type: Erratum

References (7)

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