Publication Information

{'id': 'https://openalex.org/W2066321825', 'doi': 'https://doi.org/10.1002/mds.21942', 'title': 'Two novel mutations in the <i>SPG11</i> gene causing hereditary spastic paraplegia associated with thin corpus callosum', 'display_name': 'Two novel mutations in the <i>SPG11</i> gene causing hereditary spastic paraplegia associated with thin corpus callosum', 'publication_year': 2008, 'publication_date': '2008-03-25', 'ids': {'openalex': 'https://openalex.org/W2066321825', 'doi': 'https://doi.org/10.1002/mds.21942', 'mag': '2066321825', 'pmid': 'https://pubmed.ncbi.nlm.nih.gov/18361476'}, 'language': 'en', 'primary_location': {'is_oa': True, 'landing_page_url': 'https://doi.org/10.1002/mds.21942', 'pdf_url': 'https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.21942', 'source': {'id': 'https://openalex.org/S163027424', 'display_name': 'Movement Disorders', 'issn_l': '0885-3185', 'issn': ['0885-3185', '1531-8257'], 'is_oa': False, 'is_in_doaj': False, 'is_core': True, 'host_organization': 'https://openalex.org/P4310320595', 'host_organization_name': 'Wiley', 'host_organization_lineage': ['https://openalex.org/P4310320595'], 'host_organization_lineage_names': ['Wiley'], 'type': 'journal'}, 'license': None, 'license_id': None, 'version': 'publishedVersion', 'is_accepted': True, 'is_published': True}, 'type': 'letter', 'type_crossref': 'journal-article', 'indexed_in': ['crossref', 'pubmed'], 'open_access': {'is_oa': True, 'oa_status': 'bronze', 'oa_url': 'https://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mds.21942', 'any_repository_has_fulltext': False}, 'authorships': [{'author_position': 'first', 'author': {'id': 'https://openalex.org/A5108701741', 'display_name': 'S. 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