Matches in Nanopublications for { ?s ?p "[CMT2A is an axonal autosomal dominant CMT type which in most cases is characterized by early onset and rather severe course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_assertion description "[CMT2A is an axonal autosomal dominant CMT type which in most cases is characterized by early onset and rather severe course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276200.RAQjVr24xyxjy60fkaom_9pYqcSym-uNrw3fvtS_tR82M130_provenance.
- NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_assertion description "[CMT2A is an axonal autosomal dominant CMT type which in most cases is characterized by early onset and rather severe course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1276207.RAX624SjjU1JITFo4JCdt7W7oGauNL9lPgpCC34kKNZew130_provenance.