Matches in Nanopublications for { ?s ?p "[Homozygous mutations in WWOX were reported in eight individuals of two families with autosomal recessive spinocerebellar ataxia type 12 and in two siblings with infantile epileptic encephalopathy (IEE), including one who deceased prior to DNA sampling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Homozygous mutations in WWOX were reported in eight individuals of two families with autosomal recessive spinocerebellar ataxia type 12 and in two siblings with infantile epileptic encephalopathy (IEE), including one who deceased prior to DNA sampling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1238804.RAut4XrdJdhf7TLT7KR-utx6BYS-p0fqVHdVU-9V4fbNs130_assertion description "[Homozygous mutations in WWOX were reported in eight individuals of two families with autosomal recessive spinocerebellar ataxia type 12 and in two siblings with infantile epileptic encephalopathy (IEE), including one who deceased prior to DNA sampling.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1238804.RAut4XrdJdhf7TLT7KR-utx6BYS-p0fqVHdVU-9V4fbNs130_provenance.