Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes

S. Alkindi; S. Al Zadjali; M. Al Rawahi; H. Al Haddabi; S. Daar; R. A. ElSadek; B. D. Sherkawy; A. V. Pathare

doi:10.4084/MJHID.2021.010

Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes

S. Alkindi^*, S. Al Zadjali, M. Al Rawahi, H. Al Haddabi, S. Daar, R. A. ElSadek, B. D. Sherkawy, A. V. Pathare

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

1 Citation (Scopus)

Original language	English
Article number	e2021010
Journal	Mediterranean Journal of Hematology and Infectious Diseases
Volume	13
Issue number	1
DOIs	https://doi.org/10.4084/MJHID.2021.010
Publication status	Published - Jan 2021

Keywords

Alpha thalassemia
Hemoglobin La Desirade
Sickle cell disease
Sickle cell trait
Unstable hemoglobin variant

ASJC Scopus subject areas

Hematology
Infectious Diseases

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

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10.4084/MJHID.2021.010

Cite this

Alkindi, S., Al Zadjali, S., Al Rawahi, M., Al Haddabi, H., Daar, S., ElSadek, R. A., Sherkawy, B. D., & Pathare, A. V. (2021). Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes. Mediterranean Journal of Hematology and Infectious Diseases, 13(1), Article e2021010. https://doi.org/10.4084/MJHID.2021.010

@article{187ede0089d541499f5cd17beb183390,

title = "Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes",

keywords = "Alpha thalassemia, Hemoglobin La Desirade, Sickle cell disease, Sickle cell trait, Unstable hemoglobin variant",

author = "S. Alkindi and {Al Zadjali}, S. and {Al Rawahi}, M. and {Al Haddabi}, H. and S. Daar and ElSadek, {R. A.} and Sherkawy, {B. D.} and Pathare, {A. V.}",

year = "2021",

month = jan,

doi = "10.4084/MJHID.2021.010",

language = "English",

volume = "13",

journal = "Mediterranean Journal of Hematology and Infectious Diseases",

issn = "2035-3006",

publisher = "Universita Cattolica del Sacro Cuore",

number = "1",

}

TY - JOUR

T1 - Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes

AU - Alkindi, S.

AU - Al Zadjali, S.

AU - Al Rawahi, M.

AU - Al Haddabi, H.

AU - Daar, S.

AU - ElSadek, R. A.

AU - Sherkawy, B. D.

AU - Pathare, A. V.

PY - 2021/1

Y1 - 2021/1

KW - Alpha thalassemia

KW - Hemoglobin La Desirade

KW - Sickle cell disease

KW - Sickle cell trait

KW - Unstable hemoglobin variant

UR - http://www.scopus.com/inward/record.url?scp=85099614018&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85099614018&partnerID=8YFLogxK

U2 - 10.4084/MJHID.2021.010

DO - 10.4084/MJHID.2021.010

M3 - Letter

AN - SCOPUS:85099614018

SN - 2035-3006

VL - 13

JO - Mediterranean Journal of Hematology and Infectious Diseases

JF - Mediterranean Journal of Hematology and Infectious Diseases

IS - 1

M1 - e2021010

ER -

Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes

Keywords

ASJC Scopus subject areas

UN SDGs

Access to Document

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Cite this