A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.
about
A genetic features and gene interaction study for identifying the genes that cause hereditary spherocytosis.Identification of a novel de novo ANK1 R1426* nonsense mutation in a Chinese family with hereditary spherocytosis by NGS.Targeted next-generation sequencing identifies a novel nonsense mutation in SPTB for hereditary spherocytosis: A case report of a Korean family.An ANK1 IVS3-2A>C mutation causes exon 4 skipping in two patients from a Chinese family with hereditary spherocytosis.Novel hereditary spherocytosis-associated splice site mutation in the ANK1 gene caused by parental gonosomal mosaicism.
P2860
A systematic review of hereditary spherocytosis reported in Chinese biomedical journals from 1978 to 2013 and estimation of the prevalence of the disease using a disease model.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
A systematic review of heredit ...... disease using a disease model.
@ast
A systematic review of heredit ...... disease using a disease model.
@en
type
label
A systematic review of heredit ...... disease using a disease model.
@ast
A systematic review of heredit ...... disease using a disease model.
@en
prefLabel
A systematic review of heredit ...... disease using a disease model.
@ast
A systematic review of heredit ...... disease using a disease model.
@en
P2093
P2860
P356
P1476
A systematic review of heredit ...... disease using a disease model.
@en
P2093
P2860
P356
10.5582/IRDR.2015.01002
P50
P577
2015-05-01T00:00:00Z