The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α3.7 Deletion Defect

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@article{802f4c5889734a29aca71861dd643b1c,

title = "The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α3.7 Deletion Defect",

author = "CL Harteveld and \{Van Lom\}, K and EBG Garcia and \{van Delft\}, P and PC Giordano",

year = "2003",

doi = "10.1081/HEM-120018437",

language = "English",

volume = "27",

pages = "49--51",

journal = "Hemoglobin",

issn = "0363-0269",

publisher = "Routledge/Taylor \& Francis Group",

number = "1",

}

TY - JOUR

T1 - The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α3.7 Deletion Defect

AU - Harteveld, CL

AU - Van Lom, K

AU - Garcia, EBG

AU - van Delft, P

AU - Giordano, PC

PY - 2003

Y1 - 2003

U2 - 10.1081/HEM-120018437

DO - 10.1081/HEM-120018437

M3 - Article

C2 - 12603095

SN - 0363-0269

VL - 27

SP - 49

EP - 51

JO - Hemoglobin

JF - Hemoglobin

IS - 1

ER -