Matches in Nanopublications for { ?s ?p "[Recently, we have shown that the majority of the X-linked families with infantile spasms carry mutations in the aristaless-related homeobox gene (ARX), which maps to the Xp21.3-p22.1 interval, and that the clinical picture in these patients can vary from mild mental retardation to severe ISSX with additional neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP978107.RAAlV_GbLJifXJuIK82uDwOi8zrEo9uUV2OlMTnkx-nyg130_assertion description "[Recently, we have shown that the majority of the X-linked families with infantile spasms carry mutations in the aristaless-related homeobox gene (ARX), which maps to the Xp21.3-p22.1 interval, and that the clinical picture in these patients can vary from mild mental retardation to severe ISSX with additional neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978107.RAAlV_GbLJifXJuIK82uDwOi8zrEo9uUV2OlMTnkx-nyg130_provenance.
- NP393612.RAQMnalg1_uCZ7TJ6YfNoOhdNYDeYXgx3ySX4JZTbUUog130_assertion description "[Recently, we have shown that the majority of the X-linked families with infantile spasms carry mutations in the aristaless-related homeobox gene (ARX), which maps to the Xp21.3-p22.1 interval, and that the clinical picture in these patients can vary from mild mental retardation to severe ISSX with additional neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393612.RAQMnalg1_uCZ7TJ6YfNoOhdNYDeYXgx3ySX4JZTbUUog130_provenance.
- assertion description "[Recently, we have shown that the majority of the X-linked families with infantile spasms carry mutations in the aristaless-related homeobox gene (ARX), which maps to the Xp21.3-p22.1 interval, and that the clinical picture in these patients can vary from mild mental retardation to severe ISSX with additional neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP393613.RAOhch-0hL-PStbRYnTvsnOQsW3rv5z66toLqmXz3k6IQ130_assertion description "[Recently, we have shown that the majority of the X-linked families with infantile spasms carry mutations in the aristaless-related homeobox gene (ARX), which maps to the Xp21.3-p22.1 interval, and that the clinical picture in these patients can vary from mild mental retardation to severe ISSX with additional neurological abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP393613.RAOhch-0hL-PStbRYnTvsnOQsW3rv5z66toLqmXz3k6IQ130_provenance.