Congenital transfusion-dependent anemia and thrombocytopenia with myelodysplasia due to a recurrent GATA1(G208R) germline mutation (Q80829727)

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3 January 2020

title

Congenital transfusion-dependent anemia and thrombocytopenia with myelodysplasia due to a recurrent GATA1(G208R) germline mutation (English)

1 reference

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3 January 2020

1 reference

Kratz CP

1

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3 January 2020

Niemeyer CM

2

1 reference

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3 January 2020

Karow A

3

1 reference

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3 January 2020

Volz-Fleckenstein M

4

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3 January 2020

Schmitt-Gräff A

5

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3 January 2020

Strahm B

6

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publication date

23 August 2007

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3 January 2020

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3 January 2020

volume

22

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3 January 2020

issue

2

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3 January 2020

page(s)

432-434

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https://scigraph.springernature.com/pub.10.1038/sj.leu.2404904

3 January 2020

exact match

0 references

cites work

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

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7 January 2021

X-linked thrombocytopenia caused by a novel mutation of GATA-1

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7 January 2021

Dyserythropoietic anemia and thrombocytopenia due to a novel mutation in GATA-1.

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7 January 2021

X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction

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https://api.crossref.org/works/10.1038%2FSJ.LEU.2404904

7 January 2021

X-linked gray platelet syndrome due to a GATA1 Arg216Gln mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404904

7 January 2021

Congenital erythropoietic porphyria due to a mutation in GATA1: the first trans-acting mutation causative for a human porphyria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404904

7 January 2021

Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1 mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404904

7 January 2021

Different substitutions at residue D218 of the X-linked transcription factor GATA1 lead to altered clinical severity of macrothrombocytopenia and anemia and are associated with variable skewed X inactivation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.LEU.2404904

7 January 2021

An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis

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7 January 2021