000 01656 a2200469 4500
005 20250517105754.0
264 0 _c20171207
008 201712s 0 0 eng d
022 _a1532-1681
024 7 _a10.1016/j.blre.2016.07.001
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMahdieh, Nejat
245 0 0 _aBeta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East.
_h[electronic resource]
260 _bBlood reviews
_c11 2016
300 _a493-508 p.
_bdigital
500 _aPublication Type: Journal Article; Meta-Analysis; Review
650 0 4 _aAlleles
650 0 4 _aAmino Acid Sequence
650 0 4 _aBinding Sites
650 0 4 _aComputational Biology
_xmethods
650 0 4 _aDNA Mutational Analysis
650 0 4 _aEthnicity
_xgenetics
650 0 4 _aGenetic Association Studies
650 0 4 _aHumans
650 0 4 _aIran
_xepidemiology
650 0 4 _aMiddle East
_xepidemiology
650 0 4 _aModels, Molecular
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aPolymorphism, Single Nucleotide
650 0 4 _aPopulation Surveillance
650 0 4 _aProtein Binding
650 0 4 _aProtein Conformation
650 0 4 _aProtein Interaction Mapping
650 0 4 _aProtein Interaction Maps
650 0 4 _aStructure-Activity Relationship
650 0 4 _abeta-Globins
_xchemistry
650 0 4 _abeta-Thalassemia
_xepidemiology
700 1 _aRabbani, Bahareh
773 0 _tBlood reviews
_gvol. 30
_gno. 6
_gp. 493-508
856 4 0 _uhttps://doi.org/10.1016/j.blre.2016.07.001
_zAvailable from publisher's website
999 _c26261009
_d26261009