prickle planar cell polarity protein 3 isoform 2 [Homo sapiens]

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Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder. [Am J Hum Genet. 2005]
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder.
Hudson G, Keers S, Yu-Wai-Man P, Griffiths P, Huoponen K, Savontaus ML, Nikoskelainen E, Zeviani M, Carrara F, Horvath R, et al. Am J Hum Genet. 2005 Dec; 77(6):1086-91. Epub 2005 Oct 11.
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients. [Am J Med Genet A. 2003]
X-inactivation pattern in multiple tissues from two Leber's hereditary optic neuropathy (LHON) patients.
Pegoraro E, Vettori A, Valentino ML, Molon A, Mostacciuolo ML, Howell N, Carelli V. Am J Med Genet A. 2003 May 15; 119A(1):37-40.
From genotype to phenotype in Leber hereditary optic neuropathy: still more questions than answers. [J Neuroophthalmol. 2002]
From genotype to phenotype in Leber hereditary optic neuropathy: still more questions than answers.
Newman NJ. J Neuroophthalmol. 2002 Dec; 22(4):257-61.

RefSeq genomic sequence
See the genomic reference sequence for the PRICKLE3 gene (NG_017135.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the PRICKLE3 gene (NP_006141.2).

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein