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PubCasesCollection
Documents
(1,075,899)
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# proj.
# Ann.
updated_at
PubMed
20801540
Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel g
1.84 KB
2015-11-25
34
0
-
PubMed
18046082
Identification of apolipoprotein E Guangzhou (arginine 150 proline), a new variant associated with l
1.6 KB
2015-11-23
34
0
-
PubMed
15485686
A novel SCN5A mutation manifests as a malignant form of long QT syndrome with perinatal onset of tac
1.77 KB
2015-11-19
34
0
-
PubMed
20335448
A novel point mutation in helix 10 of the human glucocorticoid receptor causes generalized glucocort
1.96 KB
2015-11-25
34
0
-
PubMed
17951029
Focal dermal hypoplasia resulting from a new nonsense mutation, p.E300X, in the PORCN gene. BACKGROU
1.48 KB
2015-11-23
34
0
-
PubMed
17910065
A novel missense mutation in the paired domain of human PAX9 causes oligodontia. PAX9 and MSX1 are t
1.13 KB
2015-11-23
34
0
-
PubMed
16781314
Ectodermal dysplasia-skin fragility syndrome resulting from a new homozygous mutation, 888delC, in t
1.02 KB
2015-11-19
34
0
-
PubMed
15609295
Compound heterozygosity for a novel nine-nucleotide deletion and the Asn45Ser missense mutation in t
1.39 KB
2015-11-18
34
0
-
PubMed
21497194
GM1 gangliosidosis and Morquio B disease: an update on genetic alterations and clinical findings. GM
1.76 KB
2015-11-26
33
0
-
PubMed
20534762
Two novel mutations of the TSH-beta subunit gene underlying congenital central hypothyroidism undete
1.82 KB
2016-01-02
33
0
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