Matches in Nanopublications for { ?s ?p "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP484552.RAZqHaZ2ZzG9UMGLVX-C2YC0TV0XYBUNF0i47C3QMjxEE130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484552.RAZqHaZ2ZzG9UMGLVX-C2YC0TV0XYBUNF0i47C3QMjxEE130_provenance.
- NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP680790.RATLUY5mNn7HU0sbDat_uy8iVwyQKy6klTaZhRnmIJhXM130_provenance.
- NP548448.RAte7m0hjUVYBDBVxTNGhHeXgrr8Ckx-bSb22T7SRhJ9Q130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548448.RAte7m0hjUVYBDBVxTNGhHeXgrr8Ckx-bSb22T7SRhJ9Q130_provenance.
- NP566859.RAr20AkNHYWtGwWre4bcluLvcN_DOl0jZQiSflJCtij8o130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566859.RAr20AkNHYWtGwWre4bcluLvcN_DOl0jZQiSflJCtij8o130_provenance.
- NP921041.RAh_EmfzYK9AdPSnq9KADN-FdRbNSMv0HokyQnZ0mOneQ130_assertion description "[Recently, mutations in the LAMB2 gene encoding laminin beta2 were described as the cause of Pierson syndrome, which is characterized by CNS and a complex ocular maldevelopment with microcoria as the most prominent clinical features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921041.RAh_EmfzYK9AdPSnq9KADN-FdRbNSMv0HokyQnZ0mOneQ130_provenance.