000 | 01957 a2200613 4500 | ||
---|---|---|---|
005 | 20250516085939.0 | ||
264 | 0 | _c20120807 | |
008 | 201208s 0 0 eng d | ||
022 | _a1932-6203 | ||
024 | 7 |
_a10.1371/journal.pone.0035015 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aKloss-Brandstätter, Anita | |
245 | 0 | 0 |
_aCandidate gene sequencing of SLC11A2 and TMPRSS6 in a family with severe anaemia: common SNPs, rare haplotypes, no causative mutation. _h[electronic resource] |
260 |
_bPloS one _c2012 |
||
300 |
_ae35015 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 |
_aAnemia, Iron-Deficiency _xblood |
650 | 0 | 4 |
_aCation Transport Proteins _xgenetics |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aDietary Supplements |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 |
_aFerritins _xblood |
650 | 0 | 4 | _aGenetic Association Studies |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 |
_aIron _xblood |
650 | 0 | 4 | _aMale |
650 | 0 | 4 |
_aMembrane Proteins _xgenetics |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aPedigree |
650 | 0 | 4 | _aPolymorphism, Single Nucleotide |
650 | 0 | 4 | _aSerbia |
650 | 0 | 4 |
_aSerine Endopeptidases _xgenetics |
700 | 1 | _aErhart, Gertraud | |
700 | 1 | _aLamina, Claudia | |
700 | 1 | _aMeister, Bernhard | |
700 | 1 | _aHaun, Margot | |
700 | 1 | _aCoassin, Stefan | |
700 | 1 | _aSeifert, Markus | |
700 | 1 | _aKlein-Franke, Andreas | |
700 | 1 | _aPaulweber, Bernhard | |
700 | 1 | _aKedenko, Lyudmyla | |
700 | 1 | _aKollerits, Barbara | |
700 | 1 | _aSwinkels, Dorine W | |
700 | 1 | _aVermeulen, Sita H | |
700 | 1 | _aGalesloot, Tessel E | |
700 | 1 | _aKronenberg, Florian | |
700 | 1 | _aWeiss, Günter | |
773 | 0 |
_tPloS one _gvol. 7 _gno. 4 _gp. e35015 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1371/journal.pone.0035015 _zAvailable from publisher's website |
999 |
_c21709028 _d21709028 |