Matches in Nanopublications for { ?s ?p "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP447480.RAPNngH2XJsB8g352ee2bPzhsmmfNx9z3-0imNq-GBWBE130_assertion description "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP447480.RAPNngH2XJsB8g352ee2bPzhsmmfNx9z3-0imNq-GBWBE130_provenance.
- assertion description "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_assertion description "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP423471.RAXf6DtYiTDlzhW0nNyOt68T1pvEencyMup5WebGNx0XE130_provenance.
- NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_assertion description "[Here, we report a family with PXE-like cutaneous features in association with multiple coagulation factor deficiency, an autosomal recessive disorder associated with GGCX mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693784.RAYAIqxnBO8z-wnnzDhCBH5qp7OsfcvJZKwmsAtvdN_5o130_provenance.