(Q24293486)

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Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene

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title

Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene (English)

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main subject

FAM20A golgi associated secretory pathway pseudokinase

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stated in

GOA release 2020-03-11

tooth eruption

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stated in

GOA release 2020-03-11

author

Rita M. Cabral

series ordinal

1

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author name string

Mazen Kurban

series ordinal

2

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Lisa Rothman

series ordinal

3

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Muhammad Wajid

series ordinal

4

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Yutaka Shimomura

series ordinal

5

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Lynn Petukhova

series ordinal

6

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Angela M Christiano

series ordinal

7

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language of work or name

English

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publication date

August 2013

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published in

Journal of Human Genetics

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volume

58

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issue

8

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page(s)

566-7

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cites work

Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndrome

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/JHG.2013.44

retrieved

20 April 2017

Novel FAM20A mutations in hypoplastic amelogenesis imperfecta

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/JHG.2013.44

retrieved

20 April 2017

FAM20: an evolutionarily conserved family of secreted proteins expressed in hematopoietic cells

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/JHG.2013.44

retrieved

20 April 2017

Mutations in FAM20C are associated with lethal osteosclerotic bone dysplasia (Raine syndrome), highlighting a crucial molecule in bone development

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/JHG.2013.44

retrieved

20 April 2017

Amelogenesis imperfecta and other biomineralization defects in Fam20a and Fam20c null mice

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038/JHG.2013.44

retrieved

20 April 2017

Defining a new candidate gene for amelogenesis imperfecta: from molecular genetics to biochemistry

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FJHG.2013.44

retrieved

21 January 2018

Identifiers

DOI

10.1038/JHG.2013.44

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Dimensions Publication ID

1009345300

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PubMed ID

23697977

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ResearchGate publication ID

236931926

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Springer Nature article ID

10.1038/jhg.2013.44

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(Q24293486)

Autosomal recessive gingival hyperplasia and dental anomalies caused by a 29-base pair duplication in the FAM20A gene

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