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1 Ergebnisse
1
EPCAM mutation update: Variants associated with congenital ..:
Pathak, Sagar J
;
Mueller, James L
;
Okamoto, Kevin
...
qt3hx9c0v4. , 2019
Link:
https://escholarship.org/uc/item/3hx9c0v4
RT Journal T1
EPCAM mutation update: Variants associated with congenital tufting enteropathy and Lynch syndrome
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt3hx9c0v4&Exemplar=1&LAN=DE A1 Pathak, Sagar J A1 Mueller, James L A1 Okamoto, Kevin A1 Das, Barun A1 Hertecant, Jozef A1 Greenhalgh, Lynn A1 Cole, Trevor A1 Pinsk, Vered A1 Yerushalmi, Baruch A1 Gurkan, Odul E A1 Yourshaw, Michael A1 Hernandez, Erick A1 Oesterreicher, Sandy A1 Naik, Sandhia A1 Sanderson, Ian R A1 Axelsson, Irene A1 Agardh, Daniel A1 Boland, C Richard A1 Martin, Martin G A1 Putnam, Christopher D A1 Sivagnanam, Mamata PB eScholarship, University of California YR 2019 K1 Biological Sciences K1 Biomedical and Clinical Sciences K1 Clinical Sciences K1 Genetics K1 Rare Diseases K1 Cancer K1 Aetiology K1 2.1 Biological and endogenous factors K1 Congenital K1 Colorectal Neoplasms K1 Hereditary Nonpolyposis K1 Diarrhea K1 Infantile K1 Epithelial Cell Adhesion Molecule K1 Epithelial Cells K1 Genetic Association Studies K1 Humans K1 Malabsorption Syndromes K1 Models K1 Molecular K1 MutS Homolog 2 Protein K1 Mutation K1 Missense K1 RNA Splice Sites K1 congenital tufting enteropathy K1 EPCAM K1 genotype-phenotype correlation K1 in silico simulation K1 Lynch syndrome K1 protein modeling K1 Genetics & Heredity JF qt3hx9c0v4 LK http://dx.doi.org/https://escholarship.org/uc/item/3hx9c0v4 DO https://escholarship.org/uc/item/3hx9c0v4 SF ELIB - SuUB Bremen
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