000 01429 a2200421 4500
005 20250514031518.0
264 0 _c20020627
008 200206s 0 0 eng d
022 _a1098-1004
024 7 _a10.1002/humu.9033
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aNajmabadi, Hossein
245 0 0 _aGJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.
_h[electronic resource]
260 _bHuman mutation
_cMay 2002
300 _a572 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 0 4 _aConnexin 26
650 0 4 _aConnexins
_xgenetics
650 0 4 _aGenes, Recessive
_xgenetics
650 0 4 _aGenetic Carrier Screening
_xmethods
650 0 4 _aGenetic Testing
_xmethods
650 0 4 _aHearing Disorders
_xgenetics
650 0 4 _aHumans
650 0 4 _aIran
_xepidemiology
650 0 4 _aMutation
_xgenetics
650 0 4 _aSyndrome
700 1 _aCucci, Robert A
700 1 _aSahebjam, Solmaz
700 1 _aKouchakian, Nafiseh
700 1 _aFarhadi, Mohammad
700 1 _aKahrizi, Kimia
700 1 _aArzhangi, Sanaz
700 1 _aDaneshmandan, Naiimeh
700 1 _aJavan, Khalil
700 1 _aSmith, Richard J H
773 0 _tHuman mutation
_gvol. 19
_gno. 5
_gp. 572
856 4 0 _uhttps://doi.org/10.1002/humu.9033
_zAvailable from publisher's website
999 _c11869735
_d11869735