(Q83396525)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22310900%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

title

Mutation identification of the DSPP in a Chinese family with DGI-II and an up-to-date bioinformatic analysis (English)

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22 January 2020

3

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22 January 2020

Bo Shen

4

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22 January 2020

author name string

Daxu Li

1

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22 January 2020

Xiaoyun Du

2

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22 January 2020

Yanli Huang

5

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22 January 2020

Robert K Valenzuela

6

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22 January 2020

Bin Wang

7

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22 January 2020

Huaxiang Zhao

8

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22 January 2020

Zunwei Liu

9

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22 January 2020

Jianjun Li

10

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22 January 2020

Zhao Xu

11

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22 January 2020

Linghan Gao

12

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22 January 2020

Jie Ma

13

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22 January 2020

publication date

31 January 2012

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22 January 2020

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22 January 2020

volume

99

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22 January 2020

issue

4

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22 January 2020

page(s)

220-226

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Hereditary dentin defects

22 January 2020

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De novo mutation in the DSPP gene associated with dentinogenesis imperfecta type II in a Japanese family

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A novel splice site mutation in the dentin sialophosphoprotein gene in a Chinese family with dentinogenesis imperfecta type II.

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A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family

7 January 2021

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Hereditary dentine disorders: dentinogenesis imperfecta and dentine dysplasia

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Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP

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A novel mutation in the DSPP gene associated with dentinogenesis imperfecta type II.

7 January 2021

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Frameshift mutations in dentin phosphoprotein and dependence of dentin disease phenotype on mutation location

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Dentin sialophosphoprotein (DSPP) is cleaved into its two natural dentin matrix products by three isoforms of bone morphogenetic protein-1 (BMP1).

7 January 2021

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7 January 2021

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7 January 2021

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Mutation of the signal peptide region of the bicistronic gene DSPP affects translocation to the endoplasmic reticulum and results in defective dentine biomineralization

7 January 2021

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Clinical, histopathologic, and genetic investigation in two large families with dentinogenesis imperfecta type II.

7 January 2021

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Mutational hot spot in the DSPP gene causing dentinogenesis imperfecta type II.

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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A novel DSPP mutation causes dentinogenesis imperfecta type II in a large Mongolian family

7 January 2021

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Overlapping DSPP mutations cause dentin dysplasia and dentinogenesis imperfecta

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

Identifiers

DOI

1 reference

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22 January 2020

1 reference