000 01397 a2200433 4500
005 20250514223631.0
264 0 _c20050503
008 200505s 0 0 eng d
022 _a1381-6810
024 7 _a10.1080/13816810590918118
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMaubaret, Cécilia
245 0 0 _aNovel mutations in MYO7A and USH2A in Usher syndrome.
_h[electronic resource]
260 _bOphthalmic genetics
_cMar 2005
300 _a25-9 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aChild
650 0 4 _aDNA Mutational Analysis
650 0 4 _aDyneins
650 0 4 _aExtracellular Matrix Proteins
_xgenetics
650 0 4 _aHearing Loss, Sensorineural
_xgenetics
650 0 4 _aHumans
650 0 4 _aMiddle Aged
650 0 4 _aMutation
_xgenetics
650 0 4 _aMyosin VIIa
650 0 4 _aMyosins
_xgenetics
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aPolymorphism, Single-Stranded Conformational
650 0 4 _aRNA Splice Sites
_xgenetics
650 0 4 _aRetinitis Pigmentosa
_xgenetics
650 0 4 _aSyndrome
700 1 _aGriffoin, Jean-Michel
700 1 _aArnaud, Bernard
700 1 _aHamel, Christian
773 0 _tOphthalmic genetics
_gvol. 26
_gno. 1
_gp. 25-9
856 4 0 _uhttps://doi.org/10.1080/13816810590918118
_zAvailable from publisher's website
999 _c15492850
_d15492850