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Benign SCA14 phenotype in a German patient associated with a missense mutation in exon 3 of the PRKCG gene
Author(s) -
Wieczorek Stefan,
Arning Larissa,
Gizewski Elke R.,
Alheite Ingrid,
Timmann Dagmar
Publication year - 2007
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.21673
Subject(s) - missense mutation , german , exon , genetics , mutation , phenotype , gene , the internet , biology , psychology , computer science , world wide web , linguistics , philosophy
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