Wirth, Brunhilde (2018). CHP1-Mutation causes cerebellar Ataxia. Med. Genet., 30 (1). S. 226 - 227. NEW YORK: SPRINGER. ISSN 1863-5490
Full text not available from this repository.| Item Type: | Journal Article | ||||||||
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| URN: | urn:nbn:de:hbz:38-194650 | ||||||||
| Journal or Publication Title: | Med. Genet. | ||||||||
| Volume: | 30 | ||||||||
| Number: | 1 | ||||||||
| Page Range: | S. 226 - 227 | ||||||||
| Date: | 2018 | ||||||||
| Publisher: | SPRINGER | ||||||||
| Place of Publication: | NEW YORK | ||||||||
| ISSN: | 1863-5490 | ||||||||
| Language: | German | ||||||||
| Faculty: | Unspecified | ||||||||
| Divisions: | Unspecified | ||||||||
| Subjects: | no entry | ||||||||
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| Refereed: | Yes | ||||||||
| URI: | http://kups.ub.uni-koeln.de/id/eprint/19465 |
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