| 000 | 01777 a2200565 4500 | ||
|---|---|---|---|
| 005 | 20250516175852.0 | ||
| 264 | 0 | _c20140929 | |
| 008 | 201409s 0 0 eng d | ||
| 022 | _a1432-198X | ||
| 024 | 7 |
_a10.1007/s00467-013-2643-0 _2doi |
|
| 040 |
_aNLM _beng _cNLM |
||
| 100 | 1 | _aWang, Yanyan | |
| 245 | 0 | 0 |
_aClinical and genetic features in autosomal recessive and X-linked Alport syndrome. _h[electronic resource] |
| 260 |
_bPediatric nephrology (Berlin, Germany) _cMar 2014 |
||
| 300 |
_a391-6 p. _bdigital |
||
| 500 | _aPublication Type: Journal Article; Research Support, Non-U.S. Gov't | ||
| 650 | 0 | 4 | _aAdolescent |
| 650 | 0 | 4 | _aAdult |
| 650 | 0 | 4 | _aDNA Mutational Analysis |
| 650 | 0 | 4 | _aFemale |
| 650 | 0 | 4 | _aGenes, X-Linked |
| 650 | 0 | 4 | _aGenetic Predisposition to Disease |
| 650 | 0 | 4 |
_aGenetic Testing _xmethods |
| 650 | 0 | 4 |
_aHearing Loss _xgenetics |
| 650 | 0 | 4 | _aHeredity |
| 650 | 0 | 4 | _aHumans |
| 650 | 0 | 4 |
_aKidney Failure, Chronic _xgenetics |
| 650 | 0 | 4 | _aMale |
| 650 | 0 | 4 | _aMiddle Aged |
| 650 | 0 | 4 | _aMutation |
| 650 | 0 | 4 |
_aNephritis, Hereditary _xcomplications |
| 650 | 0 | 4 | _aPedigree |
| 650 | 0 | 4 | _aPhenotype |
| 650 | 0 | 4 | _aPredictive Value of Tests |
| 650 | 0 | 4 | _aPrognosis |
| 650 | 0 | 4 |
_aRetinal Diseases _xgenetics |
| 650 | 0 | 4 | _aRisk Factors |
| 650 | 0 | 4 | _aSex Factors |
| 650 | 0 | 4 | _aTime Factors |
| 650 | 0 | 4 | _aYoung Adult |
| 700 | 1 | _aSivakumar, Vanessa | |
| 700 | 1 | _aMohammad, Mardhiah | |
| 700 | 1 | _aColville, Deb | |
| 700 | 1 | _aStorey, Helen | |
| 700 | 1 | _aFlinter, Frances | |
| 700 | 1 | _aDagher, Hayat | |
| 700 | 1 | _aSavige, Judy | |
| 773 | 0 |
_tPediatric nephrology (Berlin, Germany) _gvol. 29 _gno. 3 _gp. 391-6 |
|
| 856 | 4 | 0 |
_uhttps://doi.org/10.1007/s00467-013-2643-0 _zAvailable from publisher's website |
| 999 |
_c23219813 _d23219813 |
||