000 | 01309 a2200409 4500 | ||
---|---|---|---|
005 | 20250515043307.0 | ||
264 | 0 | _c20091005 | |
008 | 200910s 0 0 eng d | ||
022 | _a1750-1172 | ||
024 | 7 |
_a10.1186/1750-1172-1-40 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aHamel, Christian | |
245 | 0 | 0 |
_aRetinitis pigmentosa. _h[electronic resource] |
260 |
_bOrphanet journal of rare diseases _cOct 2006 |
||
300 |
_a40 p. _bdigital |
||
500 | _aPublication Type: Journal Article; Review | ||
650 | 0 | 4 | _aAdolescent |
650 | 0 | 4 | _aChild |
650 | 0 | 4 | _aChild, Preschool |
650 | 0 | 4 | _aDiagnosis, Differential |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 | _aInfant |
650 | 0 | 4 |
_aMetabolic Diseases _xdiagnosis |
650 | 0 | 4 |
_aNervous System Diseases _xdiagnosis |
650 | 0 | 4 |
_aNight Blindness _xdiagnosis |
650 | 0 | 4 | _aPregnancy |
650 | 0 | 4 |
_aPrenatal Diagnosis _xmethods |
650 | 0 | 4 | _aPrognosis |
650 | 0 | 4 |
_aRetinal Rod Photoreceptor Cells _xpathology |
650 | 0 | 4 |
_aRetinitis Pigmentosa _xdiagnosis |
650 | 0 | 4 |
_aRhodopsin _xgenetics |
650 | 0 | 4 |
_aSensation Disorders _xdiagnosis |
650 | 0 | 4 | _aSyndrome |
773 | 0 |
_tOrphanet journal of rare diseases _gvol. 1 _gp. 40 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1186/1750-1172-1-40 _zAvailable from publisher's website |
999 |
_c16608968 _d16608968 |