Matches in Nanopublications for { ?s ?p "[Our findings suggest that recessive ClCN7-dependent ARO may be associated with CNS involvement and have a very poor prognosis, whereas heterozygous ClCN7 mutations cause a wide range of phenotypes even in the same family, ranging from early severe to nearly asymptomatic forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP581935.RAtze0D0fewcWKd1gFburdoYQIsSCCmds4XxneSLZGeDk130_assertion description "[Our findings suggest that recessive ClCN7-dependent ARO may be associated with CNS involvement and have a very poor prognosis, whereas heterozygous ClCN7 mutations cause a wide range of phenotypes even in the same family, ranging from early severe to nearly asymptomatic forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP581935.RAtze0D0fewcWKd1gFburdoYQIsSCCmds4XxneSLZGeDk130_provenance.
- NP418657.RA3cpSHLsZP4xY5-UCOQfoSEHj__VmoOROPAhseE4BaWk130_assertion description "[Our findings suggest that recessive ClCN7-dependent ARO may be associated with CNS involvement and have a very poor prognosis, whereas heterozygous ClCN7 mutations cause a wide range of phenotypes even in the same family, ranging from early severe to nearly asymptomatic forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418657.RA3cpSHLsZP4xY5-UCOQfoSEHj__VmoOROPAhseE4BaWk130_provenance.
- NP315446.RAEFbmU-w0zUFusg6DDV9oR6spgN13Dc3ZX6QNgl-2S6M130_assertion description "[Our findings suggest that recessive ClCN7-dependent ARO may be associated with CNS involvement and have a very poor prognosis, whereas heterozygous ClCN7 mutations cause a wide range of phenotypes even in the same family, ranging from early severe to nearly asymptomatic forms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP315446.RAEFbmU-w0zUFusg6DDV9oR6spgN13Dc3ZX6QNgl-2S6M130_provenance.