000 | 01554 a2200529 4500 | ||
---|---|---|---|
005 | 20250515045802.0 | ||
264 | 0 | _c20061221 | |
008 | 200612s 0 0 eng d | ||
022 | _a1090-0535 | ||
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aVanita, Vanita | |
245 | 0 | 0 |
_aA novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin. _h[electronic resource] |
260 |
_bMolecular vision _cOct 2006 |
||
300 |
_a1217-22 p. _bdigital |
||
500 | _aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't | ||
650 | 0 | 4 |
_aAsian People _xgenetics |
650 | 0 | 4 | _aBase Sequence |
650 | 0 | 4 |
_aCataract _xcongenital |
650 | 0 | 4 | _aChild |
650 | 0 | 4 |
_aConnexins _xgenetics |
650 | 0 | 4 | _aCytosine |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 |
_aEye Proteins _xgenetics |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenes, Dominant |
650 | 0 | 4 | _aGenetic Linkage |
650 | 0 | 4 | _aGenotype |
650 | 0 | 4 | _aGuanine |
650 | 0 | 4 | _aHaplotypes |
650 | 0 | 4 | _aHeterozygote |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aIndia |
650 | 0 | 4 | _aLeucine |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMolecular Sequence Data |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 | _aProtein Structure, Tertiary |
650 | 0 | 4 | _aTranscription Initiation Site |
650 | 0 | 4 | _aValine |
700 | 1 | _aHennies, Hans Christian | |
700 | 1 | _aSingh, Daljit | |
700 | 1 | _aNürnberg, Peter | |
700 | 1 | _aSperling, Karl | |
700 | 1 | _aSingh, Jai Rup | |
773 | 0 |
_tMolecular vision _gvol. 12 _gp. 1217-22 |
|
999 |
_c16682802 _d16682802 |