A novel hemoglobin variant found on the α1 chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys).

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First Report of a Dominantly Inherited β-Thalassemia Caused by a Novel Elongated β-Globin Chain.

P2860

Q40019124-FB253953-4571-4068-9A93-B208C1DEBD44

P2860

A novel hemoglobin variant found on the α1 chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys).

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http://www.wikidata.org/entity/Q41453920

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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 novel hemoglobin variant fou ...... 8insSerHisGlySerAlaGlnValLys).

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type

Item

label

A novel hemoglobin variant fou ...... 8insSerHisGlySerAlaGlnValLys).

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A novel hemoglobin variant fou ...... 8insSerHisGlySerAlaGlnValLys).

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P1476

A novel hemoglobin variant fou ...... 58insSerHisGlySerAlaGlnValLys)

@en

P2093

Chih-Hsun Chu

http://www.w3.org/2001/XMLSchema#string

Hing-Chung Lam

http://www.w3.org/2001/XMLSchema#string

Mei-Chun Wang

http://www.w3.org/2001/XMLSchema#string

Ming-Sun Yu

http://www.w3.org/2001/XMLSchema#string

P2860

A gain-of-function mutation of JAK2 in myeloproliferative disorders

Polycythemia associated with a hemoglobinopathy

Hemoglobin olympia ( 20 valine leads to methionine): an electrophoretically silent variant associated with high oxygen affinity and erythrocytosis

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies

Classification and diagnosis of myeloproliferative neoplasms: the 2008 World Health Organization criteria and point-of-care diagnostic algorithms.

A review of variant hemoglobins interfering with hemoglobin A1c measurement.

Hemoglobin Grady: the first example of a variant with elongated chains due to an insertion of residues.

Structural and functional studies of haemoglobin Suresnes or alpha2 141 (HC3) Arg replaced by His beta2, a new high oxygen affinity mutant.

Abnormal hemoglobins with high oxygen affinity and erythrocytosis.

Hematological features and molecular lesions of hemoglobin gene disorders in Taiwanese patients.

P304

81-87

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scholarly article

P356

10.3109/03630269.2015.1005312

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Kuo-Wang Tsai

P577

2015-02-11T00:00:00Z

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272192334

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25669128

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A novel hemoglobin variant found on the α1 chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys).

about

P2860

P2860

A novel hemoglobin variant found on the α1 chain: Hb KSVGH (HBA1: p.Lys57_Gly58insSerHisGlySerAlaGlnValLys).

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P1433

P1476

P2093

P2860

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P356

P433

P478

P50

P577

P5875

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P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698