| 000 | 01552 a2200505 4500 | ||
|---|---|---|---|
| 005 | 20250514000044.0 | ||
| 264 | 0 | _c20011101 | |
| 008 | 200111s 0 0 eng d | ||
| 022 | _a1090-6576 | ||
| 024 | 7 |
_a10.1089/109065701750168806 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aNeumann, S | |
| 245 | 0 | 0 |
_aIdentification of new mutations in Israeli patients with X-linked adrenoleukodystrophy. _h[electronic resource] |
| 260 |
_bGenetic testing _c2001 |
||
| 300 |
_a65-8 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 |
_aAdrenoleukodystrophy _xgenetics |
| 650 | 0 | 4 |
_aArabs _xgenetics |
| 650 | 0 | 4 | _aBase Sequence |
| 650 | 0 | 4 |
_aCodon, Nonsense _xgenetics |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aExons |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aFounder Effect |
| 650 | 0 | 4 |
_aFrameshift Mutation _xgenetics |
| 650 | 0 | 4 |
_aGenetic Linkage _xgenetics |
| 650 | 0 | 4 | _aHeterozygote |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 | _aIsrael |
| 650 | 0 | 4 |
_aJews _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 |
_aMorocco _xethnology |
| 650 | 0 | 4 |
_aMutation _xgenetics |
| 650 | 0 | 4 |
_aMutation, Missense _xgenetics |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 |
_aX Chromosome _xgenetics |
| 700 | 1 | _aTopper, A | |
| 700 | 1 | _aMandel, H | |
| 700 | 1 | _aShapira, I | |
| 700 | 1 | _aGolan, O | |
| 700 | 1 | _aGazit, E | |
| 700 | 1 | _aLoewenthal, R | |
| 773 | 0 |
_tGenetic testing _gvol. 5 _gno. 1 _gp. 65-8 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1089/109065701750168806 _zAvailable from publisher's website |
| 999 |
_c11269515 _d11269515 |
||