000			01879 a2200553 4500
005			20250516171001.0
264		0	_c20131216
008			201312s 0 0 eng d
022			_a1479-683X
024	7		_a10.1530/EJE-13-0419 _2doi
040			_aNLM _beng _cNLM
100	1		_aSarfati, Julie
245	0	0	_aGreater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients. _h[electronic resource]
260			_bEuropean journal of endocrinology _cDec 2013
300			_a805-9 p. _bdigital
500			_aPublication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdult
650	0	4	_aAfrica, Northern
650	0	4	_aAged
650	0	4	_aArabs _xgenetics
650	0	4	_aEurope
650	0	4	_aExons
650	0	4	_aExtracellular Matrix Proteins _xgenetics
650	0	4	_aFemale
650	0	4	_aFibroblast Growth Factor 8 _xgenetics
650	0	4	_aGastrointestinal Hormones _xgenetics
650	0	4	_aGene Frequency
650	0	4	_aHumans
650	0	4	_aIntrons
650	0	4	_aKallmann Syndrome _xepidemiology
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aMutation
650	0	4	_aNerve Tissue Proteins _xgenetics
650	0	4	_aNeuropeptides _xgenetics
650	0	4	_aPrevalence
650	0	4	_aReceptor, Fibroblast Growth Factor, Type 1 _xgenetics
650	0	4	_aReceptors, G-Protein-Coupled _xgenetics
650	0	4	_aReceptors, Peptide _xgenetics
650	0	4	_aSequence Analysis, DNA
650	0	4	_aWhite People _xgenetics
700	1		_aFouveaut, Corinne
700	1		_aLeroy, Chrystel
700	1		_aJeanpierre, Marc
700	1		_aHardelin, Jean-Pierre
700	1		_aDodé, Catherine
773	0		_tEuropean journal of endocrinology _gvol. 169 _gno. 6 _gp. 805-9
856	4	0	_uhttps://doi.org/10.1530/EJE-13-0419 _zAvailable from publisher's website
999			_c23083386 _d23083386