Variant: rs267608216 

    present in Gene: PEX6
    present in Chromosome: 6
    Position on Chromosome: 42969714
    Alleles of this Variant: CCAGGCCT/-

rs267608216 in PEX6 gene and HEIMLER SYNDROME 2 PMID 19877282 2010 Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients.

PMID 27302843 2016 Spectrum of PEX1 and PEX6 variants in Heimler syndrome.

PMID 19142205 2009 Rational diagnostic strategy for Zellweger syndrome spectrum patients.

rs267608216 in PEX6 gene and PEROXISOME BIOGENESIS DISORDER 4A (ZELLWEGER) PMID 27302843 2016 Spectrum of PEX1 and PEX6 variants in Heimler syndrome.

PMID 19877282 2010 Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients.

PMID 24016303 2013 Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder.

PMID 19142205 2009 Rational diagnostic strategy for Zellweger syndrome spectrum patients.

rs267608216 in PEX6 gene and PEROXISOME BIOGENESIS DISORDER 4B PMID 19142205 2009 Rational diagnostic strategy for Zellweger syndrome spectrum patients.

PMID 19877282 2010 Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients.

rs267608216 in PEX6 gene and Peroxisome biogenesis disorders PMID 19142205 2009 Rational diagnostic strategy for Zellweger syndrome spectrum patients.

PMID 19877282 2010 Spectrum of PEX6 mutations in Zellweger syndrome spectrum patients.

PMID 24016303 2013 Arginine improves peroxisome functioning in cells from patients with a mild peroxisome biogenesis disorder.

PMID 27302843 2016 Spectrum of PEX1 and PEX6 variants in Heimler syndrome.