Matches in Nanopublications for { ?s ?p "[Heterozygous loss-of-function mutations in AFG3L2 cause autosomal-dominant spinocerebellar ataxia type 28 (SCA28), a disorder whose phenotype is strikingly different from that of our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP856470.RAQgQM5CtpWZ5dell67SMi2fKyqBhIFDoCCh704eowpog130_assertion description "[Heterozygous loss-of-function mutations in AFG3L2 cause autosomal-dominant spinocerebellar ataxia type 28 (SCA28), a disorder whose phenotype is strikingly different from that of our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP856470.RAQgQM5CtpWZ5dell67SMi2fKyqBhIFDoCCh704eowpog130_provenance.
- NP471673.RAMZrkucRSGjXNUMp3QCv4G_U0piyGYq00ZiS5nDnSbAQ130_assertion description "[Heterozygous loss-of-function mutations in AFG3L2 cause autosomal-dominant spinocerebellar ataxia type 28 (SCA28), a disorder whose phenotype is strikingly different from that of our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471673.RAMZrkucRSGjXNUMp3QCv4G_U0piyGYq00ZiS5nDnSbAQ130_provenance.
- assertion description "[Heterozygous loss-of-function mutations in AFG3L2 cause autosomal-dominant spinocerebellar ataxia type 28 (SCA28), a disorder whose phenotype is strikingly different from that of our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Heterozygous loss-of-function mutations in AFG3L2 cause autosomal-dominant spinocerebellar ataxia type 28 (SCA28), a disorder whose phenotype is strikingly different from that of our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP933161.RATb9m9nPCEBvwYCYRpyQwgCViBvHQTtTQYW7Br0HRHDk130_assertion description "[Heterozygous loss-of-function mutations in AFG3L2 cause autosomal-dominant spinocerebellar ataxia type 28 (SCA28), a disorder whose phenotype is strikingly different from that of our patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP933161.RATb9m9nPCEBvwYCYRpyQwgCViBvHQTtTQYW7Br0HRHDk130_provenance.