000 | 01377 a2200397 4500 | ||
---|---|---|---|
005 | 20250516003058.0 | ||
264 | 0 | _c20101025 | |
008 | 201010s 0 0 eng d | ||
022 | _a1421-9662 | ||
024 | 7 |
_a10.1159/000318737 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aKutlar, Ferdane | |
245 | 0 | 0 |
_aA new sickling variant 'Hb S-Wake β[(Glu6Val-Asn139 Ser)]' found in a compound heterozygote with Hb S β(Glu6Val) coinherited with homozygous α-thalassemia-2: phenotype and molecular characteristics. _h[electronic resource] |
260 |
_bActa haematologica _c2010 |
||
300 |
_a120-4 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 |
_aAnemia, Sickle Cell _xcomplications |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 | _aGenetic Variation |
650 | 0 | 4 |
_aHemoglobin, Sickle _xchemistry |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHomozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aProtein Structure, Tertiary |
650 | 0 | 4 |
_aalpha-Thalassemia _xcomplications |
700 | 1 | _aRedding-Lallinger, R | |
700 | 1 | _aMeiler, S E | |
700 | 1 | _aBakanay, S M | |
700 | 1 | _aBorders, L | |
700 | 1 | _aKutlar, A | |
773 | 0 |
_tActa haematologica _gvol. 124 _gno. 2 _gp. 120-4 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1159/000318737 _zAvailable from publisher's website |
999 |
_c20191557 _d20191557 |