Matches in Nanopublications for { ?s ?p "[We set out to measure the frequency of sequence variants in PAK3 in schizophrenia without premorbid MR. We conducted complete gene reseqeuncing of all coding exons and exon-intron boundaries in patients with schizophrenia with cognitive impairment but without premorbid MR. Deleterious variants in schizophrenia alone were rare (<1/159 or 0.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP636245.RAjYrosJ9LvCdTiv31wGFNyEo7SwhNllOnBvyf6XdljLA130_assertion description "[We set out to measure the frequency of sequence variants in PAK3 in schizophrenia without premorbid MR. We conducted complete gene reseqeuncing of all coding exons and exon-intron boundaries in patients with schizophrenia with cognitive impairment but without premorbid MR. Deleterious variants in schizophrenia alone were rare (<1/159 or 0.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP636245.RAjYrosJ9LvCdTiv31wGFNyEo7SwhNllOnBvyf6XdljLA130_provenance.
- NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_assertion description "[We set out to measure the frequency of sequence variants in PAK3 in schizophrenia without premorbid MR. We conducted complete gene reseqeuncing of all coding exons and exon-intron boundaries in patients with schizophrenia with cognitive impairment but without premorbid MR. Deleterious variants in schizophrenia alone were rare (<1/159 or 0.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750648.RAsmDRxLd057gI_gtYzxV10UIejc6ZN7o0ymJUrQ7GM1c130_provenance.
- NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_assertion description "[We set out to measure the frequency of sequence variants in PAK3 in schizophrenia without premorbid MR. We conducted complete gene reseqeuncing of all coding exons and exon-intron boundaries in patients with schizophrenia with cognitive impairment but without premorbid MR. Deleterious variants in schizophrenia alone were rare (<1/159 or 0.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169571.RAxfUwsPbL99-DXWm2U8PERMKLnMp-xrCFhYx9y3fmHrk130_provenance.