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UnknownPathogenic potential of emergent sorbitol-fermenting Escherichia coli O157:NM.
Not available
S-EPMC2583558 | biostudies-literature
UnknownRefining Genotype-Phenotype Correlation in Autosomal Dominant Polycystic Kidney Disease.
Not available
S-EPMC4884120 | biostudies-literature
UnknownShwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.
Not available
S-EPMC1275624 | biostudies-literature
UnknownTrans-ancestry meta-analysis of genome wide association studies of inhibitory control.
Not available
S-EPMC10827666 | biostudies-literature
UnknownPMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia.
Not available
S-EPMC4542620 | biostudies-literature
UnknownMutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
Not available
S-EPMC1698556 | biostudies-literature
UnknownIdentification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Not available
S-EPMC4133584 | biostudies-literature
UnknownJMJD6 promotes self-renewal and regenerative capacity of hematopoietic stem cells.
Not available
S-EPMC7876897 | biostudies-literature
UnknownFatal COVID-19 outcomes are associated with an antibody response targeting epitopes shared with endemic coronaviruses.
Not available
S-EPMC9310533 | biostudies-literature
UnknownAutosomal dominant non-syndromic hearing loss maps to DFNA33 (13q34) and co-segregates with splice and frameshift variants in ATP11A, a phospholipid flippase gene.
Not available
S-EPMC9035003 | biostudies-literature
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