000 01049 a2200277 4500
005 20250516184251.0
264 0 _c20140814
008 201408s 0 0 fre d
022 _a0151-9638
024 7 _a10.1016/j.annder.2013.08.004
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDereure, O
245 0 0 _a[Autosomal dominant (familial) infantile myofibromatosis: The causative role of mutations in PDGFRB and NOTCH3].
_h[electronic resource]
260 _bAnnales de dermatologie et de venereologie
_cDec 2013
300 _a833-4 p.
_bdigital
500 _aPublication Type: Journal Article; Comment
650 0 4 _aFemale
650 0 4 _aGenes, Dominant
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation, Missense
650 0 4 _aMyofibromatosis
_xcongenital
650 0 4 _aReceptor, Platelet-Derived Growth Factor beta
_xgenetics
773 0 _tAnnales de dermatologie et de venereologie
_gvol. 140
_gno. 12
_gp. 833-4
856 4 0 _uhttps://doi.org/10.1016/j.annder.2013.08.004
_zAvailable from publisher's website
999 _c23345409
_d23345409