000 01596 a2200493 4500
005 20250515134621.0
264 0 _c20090825
008 200908s 0 0 eng d
022 _a1879-1484
024 7 _a10.1016/j.atherosclerosis.2008.07.026
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aFaiyaz-Ul-Haque, Muhammad
245 0 0 _aA novel missense and a recurrent mutation in SLC2A10 gene of patients affected with arterial tortuosity syndrome.
_h[electronic resource]
260 _bAtherosclerosis
_cApr 2009
300 _a466-71 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aArteries
_xpathology
650 0 4 _aConnective Tissue Diseases
_xgenetics
650 0 4 _aConstriction, Pathologic
650 0 4 _aDNA Mutational Analysis
650 0 4 _aFamily Health
650 0 4 _aFemale
650 0 4 _aGlucose Transport Proteins, Facilitative
_xgenetics
650 0 4 _aHomozygote
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aMutation, Missense
650 0 4 _aPhenotype
650 0 4 _aSaudi Arabia
650 0 4 _aSyndrome
700 1 _aZaidi, Syed H E
700 1 _aAl-Sanna, Nouriyah
700 1 _aAlswaid, Abdulrahman
700 1 _aMomenah, Tariq
700 1 _aKaya, Namik
700 1 _aAl-Dayel, Fouad
700 1 _aBouhoaigah, Issam
700 1 _aSaliem, Mohammed
700 1 _aTsui, Lap-Chee
700 1 _aTeebi, Ahmad S
773 0 _tAtherosclerosis
_gvol. 203
_gno. 2
_gp. 466-71
856 4 0 _uhttps://doi.org/10.1016/j.atherosclerosis.2008.07.026
_zAvailable from publisher's website
999 _c18243843
_d18243843