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