Matches in Nanopublications for { ?s ?p "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 10 of
10
with 100 items per page.
- assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP7917.RAUAKJOyeCZvjI56_58s4Xxk7pgQKj6NCn2WNIzQYmtuo130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7917.RAUAKJOyeCZvjI56_58s4Xxk7pgQKj6NCn2WNIzQYmtuo130_provenance.
- NP48966.RA1BloyvaKp1_wl0_crpdDn4JqtZSQnxvneEeAgRLRdtE130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP48966.RA1BloyvaKp1_wl0_crpdDn4JqtZSQnxvneEeAgRLRdtE130_provenance.
- NP59936.RAY3cwaQt5_AtciidSL5kZwMnPjZoD42P_eSmagRDhRIY130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP59936.RAY3cwaQt5_AtciidSL5kZwMnPjZoD42P_eSmagRDhRIY130_provenance.
- NP191491.RACjcmFTKrCI3CNpfLwHMyzQk5054KcST5HW7-AWAnK9Y130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP191491.RACjcmFTKrCI3CNpfLwHMyzQk5054KcST5HW7-AWAnK9Y130_provenance.
- NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP864997.RAMJtOJBqfjAPTVhCkRvkFCYBLRxb3A1DlknqpP6WtO7I130_provenance.
- NP228425.RAohzWqFt1D0B9fzT9PW3tCyNyAFDks--llSAkbKX_Ky8130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP228425.RAohzWqFt1D0B9fzT9PW3tCyNyAFDks--llSAkbKX_Ky8130_provenance.
- NP37365.RAGJvGCBJPK00vejBCuwYU9No7BA1gDzCOCbJXPYe8b68130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP37365.RAGJvGCBJPK00vejBCuwYU9No7BA1gDzCOCbJXPYe8b68130_provenance.
- NP1365491.RAK7oZv6_uxcDMMxh8KUQBRNDWCtvAoz9pmKeZJDRshHA130_assertion description "[A nonsense mutation due to a single base insertion in the 3'-coding region of glycogen debranching enzyme gene associated with a severe phenotype in a patient with glycogen storage disease type IIIa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1365491.RAK7oZv6_uxcDMMxh8KUQBRNDWCtvAoz9pmKeZJDRshHA130_provenance.