Matches in Nanopublications for { ?s ?p "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP699691.RArMFj7Rt-TdhUdNi1LTJuSzj6oj0uRvVhDUgQtLPlpsc130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP699691.RArMFj7Rt-TdhUdNi1LTJuSzj6oj0uRvVhDUgQtLPlpsc130_provenance.
- assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP924969.RA-4KBP32Iv5Xn82ft4tgtgHPU_nIlhVz-X2CYIrG91AE130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924969.RA-4KBP32Iv5Xn82ft4tgtgHPU_nIlhVz-X2CYIrG91AE130_provenance.
- NP269675.RAqGJMgmrvzOWC-BYZzSlJbIszVGGwLyENGS8349pIdQo130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269675.RAqGJMgmrvzOWC-BYZzSlJbIszVGGwLyENGS8349pIdQo130_provenance.
- NP889344.RAsk8oOD2GYzmwyJCPouq9LTsn-42cj9qo4mXjZANf4_w130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP889344.RAsk8oOD2GYzmwyJCPouq9LTsn-42cj9qo4mXjZANf4_w130_provenance.
- NP366610.RA-uMV4hbYgALKM7sYWsprd3bZ2tUhUr8ij5kFCJwNzb8130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP366610.RA-uMV4hbYgALKM7sYWsprd3bZ2tUhUr8ij5kFCJwNzb8130_provenance.
- NP531.RA1erQMmVZfqTeodbuEvwITAs5QcoIukSEG1Pe5e3dYDw130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP531.RA1erQMmVZfqTeodbuEvwITAs5QcoIukSEG1Pe5e3dYDw130_provenance.
- NP269678.RA-QEz_bD0K5ay6fHzffOiIDhQm97qLrwKjaI2KSLCLxw130_assertion description "[Identification of a novel mutation R42P in the gap junction protein beta-3 associated with autosomal dominant erythrokeratoderma variabilis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP269678.RA-QEz_bD0K5ay6fHzffOiIDhQm97qLrwKjaI2KSLCLxw130_provenance.