King Tutankhamun's family and demise

JAMA

Volumn 303, Issue 24, 2010, Pages 2473-

  Timmann, Christian ^a   Meyer, Christian G ^a  

^a BERNHARD NOCHT INSTITUTE FOR TROPICAL MEDICINE   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

BETA THALASSEMIA; BONE NECROSIS; CLINICAL FEATURE; DISEASE COURSE; DISEASE SEVERITY; ENDEMIC DISEASE; GENE; GENE MUTATION; HETEROZYGOSITY; HOMOZYGOSITY; INFECTION; LETTER; MALARIA; OSTEOMYELITIS; PRIORITY JOURNAL; SCD GENE; SICKLE CELL ANEMIA;

EID: 77953853049     PISSN: 00987484     EISSN: 15383598     Source Type: Journal    
DOI: 10.1001/jama.2010.822     Document Type: Letter

References (5)

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3. El-Beshlawy A, Youssry I. Prevention of hemoglobinopathies in Egypt. Hemoglobin. 2009;33(suppl 1):S14-S20.
4. Makani J, Komba AN, Cox SE, et al. Malaria in patients with sickle cell anemia: burden, risk factors, and outcome at the outpatient clinic and during hospitalization. Blood. 2010;115(2):215-220.
5. Williams TN, Mwangi TW,Wambua S, et al. Sickle cell trait and the risk of Plasmodium falciparum malaria and other childhood diseases. J Infect Dis. 2005; 192(1):178-186.