Matches in Nanopublications for { ?s ?p "[In addition, cerebellar hypoplasia and Walcott-Rallison syndrome have been associated with PNDM, suggesting an autosomal recessive inheritance pattern; furthermore, a mutation in the gene insulin promoter factor 1 has been identified as a cause of pancreatic agenesis in PNDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_assertion description "[In addition, cerebellar hypoplasia and Walcott-Rallison syndrome have been associated with PNDM, suggesting an autosomal recessive inheritance pattern; furthermore, a mutation in the gene insulin promoter factor 1 has been identified as a cause of pancreatic agenesis in PNDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP815967.RASj7ewmGtY3RF3OiphujNh5D-MfrZzfXc6X_OrDA2LG0130_provenance.