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Journal Article|Review |
| endingPage |
230 |
| issn |
0920-1211 |
| pageRange |
S223-230 |
| publicationName |
Epilepsy Research |
| startingPage |
S223 |
| bibliographicCitation |
Fujiwara T. Clinical spectrum of mutations in SCN1A gene: severe myoclonic epilepsy in infancy and related epilepsies. Epilepsy Res. 2006 Aug;70 Suppl 1():S223–30. doi: 10.1016/j.eplepsyres.2006.01.019. PMID: 16806826. |
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_9da7f3174cd64b4cd0a511655ea4d376 |
| date |
200608 |
| identifier |
https://pubmed.ncbi.nlm.nih.gov/16806826
https://doi.org/10.1016/j.eplepsyres.2006.01.019 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3587
https://portal.issn.org/resource/ISSN/0920-1211 |
| language |
English |
| source |
https://pubmed.ncbi.nlm.nih.gov/
https://www.crossref.org/ |
| title |
Clinical spectrum of mutations in SCN1A gene: Severe myoclonic epilepsy in infancy and related epilepsies |
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