unnamed protein product [Homo sapiens]

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Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature review. [Am J Med Genet A. 2015]
Phenotypic variation of TTC19-deficient mitochondrial complex III deficiency: a case report and literature review.
Mordaunt DA, Jolley A, Balasubramaniam S, Thorburn DR, Mountford HS, Compton AG, Nicholl J, Manton N, Clark D, Bratkovic D, et al. Am J Med Genet A. 2015 Jun; 167(6):1330-6. Epub 2015 Apr 21.
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype. [Orphanet J Rare Dis. 2015]
Mutations in TTC19: expanding the molecular, clinical and biochemical phenotype.
Koch J, Freisinger P, Feichtinger RG, Zimmermann FA, Rauscher C, Wagentristl HP, Konstantopoulou V, Seidl R, Haack TB, Prokisch H, et al. Orphanet J Rare Dis. 2015 Apr 2; 10:40. Epub 2015 Apr 2.
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient. [BMC Neurol. 2014]
Exome sequencing reveals a novel TTC19 mutation in an autosomal recessive spinocerebellar ataxia patient.
Morino H, Miyamoto R, Ohnishi S, Maruyama H, Kawakami H. BMC Neurol. 2014 Jan 7; 14:5. Epub 2014 Jan 7.

RefSeq genomic sequence
See the genomic reference sequence for the TTC19 gene (NG_029806.2).
RefSeq protein isoforms
See 8 reference sequence protein isoforms for the TTC19 gene.

Nucleotide
Nucleotide sequence from coding region
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