Matches in Nanopublications for { ?s ?p "[We suggest that EXOSC3 mutations may present not only as pontocerebellar hypoplasia type 1, but also as a complicated form of hereditary spastic paraplegia without pontine hypoplasia or atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[We suggest that EXOSC3 mutations may present not only as pontocerebellar hypoplasia type 1, but also as a complicated form of hereditary spastic paraplegia without pontine hypoplasia or atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_assertion description "[We suggest that EXOSC3 mutations may present not only as pontocerebellar hypoplasia type 1, but also as a complicated form of hereditary spastic paraplegia without pontine hypoplasia or atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1213009.RAKIbRM2LlztCDUsQBI4tJdFtfU23Wq82I2qZsmTd0coM130_provenance.