Matches in Nanopublications for { ?s ?p "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP939306.RAbG5w-wFsm-449NroeBQjdEseb_GqavBFFCWi04toR1Q130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP939306.RAbG5w-wFsm-449NroeBQjdEseb_GqavBFFCWi04toR1Q130_provenance.
- NP439799.RAkrJr7-ng4-qEjgCMp6-Wmh3Kn4mdPlGQweMjjY_cPOI130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP439799.RAkrJr7-ng4-qEjgCMp6-Wmh3Kn4mdPlGQweMjjY_cPOI130_provenance.
- NP194658.RA-NX8z_vkSVDElTLq8cZDPk9Ic_K9soo9VcFZypTROCQ130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP194658.RA-NX8z_vkSVDElTLq8cZDPk9Ic_K9soo9VcFZypTROCQ130_provenance.
- assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP735245.RAXtRn-Y9prch0fiecrgVLpyHZq2csH_BxcrM8IlqDTOs130_provenance.
- assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP403884.RAdSXFy-gNa8uslPPeq5zwXiCiDR-KnwoBF--DFDTZiXI130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403884.RAdSXFy-gNa8uslPPeq5zwXiCiDR-KnwoBF--DFDTZiXI130_provenance.
- NP420588.RAqz_ii_R0A9sUIXuXALS3mpQoSkfdBiF_Npc2yq6Ovqw130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420588.RAqz_ii_R0A9sUIXuXALS3mpQoSkfdBiF_Npc2yq6Ovqw130_provenance.
- NP403882.RAPp0pcA_Hz-ICURWMViOJGNXZSL5TE6YEtY9GsricAVU130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403882.RAPp0pcA_Hz-ICURWMViOJGNXZSL5TE6YEtY9GsricAVU130_provenance.
- NP403880.RA_yCu5RKiUYPAtnbptDWLtvnn3FlN76_tZwxXn9HTj2c130_assertion description "[Recessively inherited deficiency of TH was recently identified and incorporated into recent concepts of genetic dystonias as the cause of recessive Dopa-responsive dystonia or Segawa's syndrome in analogy to dominantly inherited GTP cyclohydrolase I deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP403880.RA_yCu5RKiUYPAtnbptDWLtvnn3FlN76_tZwxXn9HTj2c130_provenance.