000 01550 a2200433 4500
005 20250516093559.0
264 0 _c20121001
008 201210s 0 0 eng d
022 _a1442-200X
024 7 _a10.1111/j.1442-200X.2011.03482.x
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDensupsoontorn, Narumon
245 0 0 _aImerslund-Gräsbeck syndrome: new mutation in amnionless.
_h[electronic resource]
260 _bPediatrics international : official journal of the Japan Pediatric Society
_cJun 2012
300 _ae19-21 p.
_bdigital
500 _aPublication Type: Case Reports; Journal Article
650 0 4 _aAnemia, Megaloblastic
650 0 4 _aChild, Preschool
650 0 4 _aHumans
650 0 4 _aMalabsorption Syndromes
_xgenetics
650 0 4 _aMale
650 0 4 _aMembrane Proteins
650 0 4 _aMutation
650 0 4 _aProteins
_xgenetics
650 0 4 _aProteinuria
_xgenetics
650 0 4 _aVitamin B 12 Deficiency
_xgenetics
700 1 _aSanpakit, Kleebsabai
700 1 _aVijarnsorn, Chodchanok
700 1 _aPattaragarn, Aniruth
700 1 _aKangwanpornsiri, Channagarn
700 1 _aJatutipsompol, Charnnarong
700 1 _aTirapongporn, Hathaichanok
700 1 _aJirapinyo, Pipop
700 1 _aShah, Nidhi P
700 1 _aSturm, Amy C
700 1 _aTanner, Stephan M
773 0 _tPediatrics international : official journal of the Japan Pediatric Society
_gvol. 54
_gno. 3
_gp. e19-21
856 4 0 _uhttps://doi.org/10.1111/j.1442-200X.2011.03482.x
_zAvailable from publisher's website
999 _c21811785
_d21811785