Myoclonus-dystonia: significance of large SGCE deletions.

Human mutation

Volumn 29, Issue 2, 2008, Pages 331-332

  Grunewald A ^a   Djarmati, A ^a   Lohmann Hedrich, K ^a   Farrell, K ^a   Zeller, J A ^a   Allert, N ^a   Papengut, F ^a   Petersen, B ^a   Fung, V ^a   Sue, C M ^a   O'Sullivan, D ^a   Mahant, N ^a   Kupsch, A ^a   Chuang, R S ^a   Wiegers, K ^a   Pawlack, H ^a   Hagenah, J ^a   Ozelius, L J ^a   Stephani, U ^a   Schuit, R ^a   Lang, A E ^a   Volkmann, J ^a   Munchau A ^a   Klein, C ^a   more..

^a UNIVERSITY OF LÜBECK   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

SARCOGLYCAN;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; DEMOGRAPHY; EXON; FEMALE; GENE DELETION; GENETICS; GENOME; HUMAN; LITERATURE; MALE; MIDDLE AGED; MOLECULAR GENETICS; MYOCLONUS; NUCLEOTIDE SEQUENCE; PEDIGREE; PHENOTYPE; PRESCHOOL CHILD;

ADOLESCENT; ADULT; AGED; BASE SEQUENCE; CHILD; CHILD, PRESCHOOL; DEMOGRAPHY; DNA MUTATIONAL ANALYSIS; EXONS; FEMALE; GENE DELETION; GENOME, HUMAN; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MYOCLONUS; PEDIGREE; PHENOTYPE; REVIEW LITERATURE AS TOPIC; SARCOGLYCANS;

EID: 38949166903     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9521     Document Type: Article

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