Matches in Nanopublications for { ?s ?p "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257193.RAxHaW_3wCtUrr6vRHWEUMwCx1h-_MVEll4RbkRqzPWYo130_provenance.
- assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP257188.RAY8Xbxiwh8edPH7DHV5fevGVJ1R-_eUUdUcm2PxpMQzw130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257188.RAY8Xbxiwh8edPH7DHV5fevGVJ1R-_eUUdUcm2PxpMQzw130_provenance.
- assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541605.RAjRTB3qC1IUYgpf5av0lWG-gdlqSeC5ekLx2zxgx6DpE130_provenance.
- NP681476.RAoKDNLkHdSHAReSaggXqchZU-qwsgr6xcSQPvF4gRdVs130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681476.RAoKDNLkHdSHAReSaggXqchZU-qwsgr6xcSQPvF4gRdVs130_provenance.
- NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681675.RAm48_LqQs2qTY9h50HCQh6Jj2uL357Xsl_rySjG_UEY0130_provenance.
- NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_assertion description "[Clinical and molecular studies of 73 Italian families with autosomal dominant cerebellar ataxia type I: SCA1 and SCA2 are the most common genotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP257187.RApNe_fFX178pRxD_xsRIxWxKIC0DxEcO-8OzRlGHioWg130_provenance.