000 01161 a2200337 4500
005 20250515205132.0
264 0 _c20101220
008 201012s 0 0 eng d
022 _a1751-553X
024 7 _a10.1111/j.1751-553X.2009.01217.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aAngalena, R
245 0 0 _aA novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta-globin gene leads to thalassemia major.
_h[electronic resource]
260 _bInternational journal of laboratory hematology
_cOct 2010
300 _a548-9 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aChild
650 0 4 _aFemale
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aPoint Mutation
650 0 4 _abeta-Globins
_xgenetics
650 0 4 _abeta-Thalassemia
_xgenetics
700 1 _aPrabitha, K N
700 1 _aChaudhary, A K
700 1 _aBashyam, M D
700 1 _aJain, S
700 1 _aDalal, A B
773 0 _tInternational journal of laboratory hematology
_gvol. 32
_gno. 5
_gp. 548-9
856 4 0 _uhttps://doi.org/10.1111/j.1751-553X.2009.01217.x
_zAvailable from publisher's website
999 _c19508189
_d19508189