Severe Hb H Disease Caused by Hb Zürich-Albisrieden (<i>HBA1</i>: c.178G>C): Another Case Report.

Wu, Shao-Min; Huang, Su-Ran; Li, Chan; Chen, Gui-Lan; Li, Dong-Zhi

Severe Hb H Disease Caused by Hb Zürich-Albisrieden (HBA1: c.178G>C): Another Case Report.

Wu, Shao-Min; Huang, Su-Ran; Li, Chan; Chen, Gui-Lan; Li, Dong-Zhi.

Afiliación

Wu SM; Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong Province, People's Republic of China.
Huang SR; Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong Province, People's Republic of China.
Li C; Prenatal Diagnosis Center, Affiliated Dongguan Hospital, Southern Medical University (Dongguan People's Hospital), Dongguan, Guangdong Province, People's Republic of China.
Chen GL; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China.
Li DZ; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China.

Hemoglobin ; 46(6): 341-343, 2022 Nov.

Article en En | MEDLINE | ID: mdl-36815319

Asunto(s)

Anemia; Hemoglobinas Anormales; Talasemia alfa; Humanos; Hemoglobina Glucada; Talasemia alfa/genética; Hemoglobinas Anormales/genética; Mutación; Globinas alfa/genética

Palabras clave

Hb H disease; Hb ZürichAlbisrieden; Hb variant; α-Thalassemia (α-thal)

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Hemoglobinas Anormales / Talasemia alfa / Anemia Límite: Humans Idioma: En Revista: Hemoglobin Año: 2022 Tipo del documento: Article Pais de publicación: Reino Unido

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