rs121918658
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.
|
22410471 |
2012 |
rs121918658
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1-associated Leigh syndrome: a case series and novel mutations.
|
22488715 |
2012 |
rs28933402
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1-associated Leigh syndrome: a case series and novel mutations.
|
22488715 |
2012 |
rs28933402
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.
|
22410471 |
2012 |
rs398122806
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.
|
22410471 |
2012 |
rs398122806
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1-associated Leigh syndrome: a case series and novel mutations.
|
22488715 |
2012 |
rs782024654
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1-associated Leigh syndrome: a case series and novel mutations.
|
22488715 |
2012 |
rs782024654
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.
|
22410471 |
2012 |
rs782033035
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Two Japanese patients with Leigh syndrome caused by novel SURF1 mutations.
|
22410471 |
2012 |
rs782033035
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1-associated Leigh syndrome: a case series and novel mutations.
|
22488715 |
2012 |
rs121918658
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
|
21937992 |
2011 |
rs28933402
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
|
21937992 |
2011 |
rs398122806
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
|
21937992 |
2011 |
rs782024654
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
|
21937992 |
2011 |
rs782033035
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
|
21937992 |
2011 |
rs121918658
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1 gene mutations in Polish patients with COX-deficient Leigh syndrome.
|
14564068 |
2001 |
rs28933402
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1 gene mutations in Polish patients with COX-deficient Leigh syndrome.
|
14564068 |
2001 |
rs398122806
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1 gene mutations in Polish patients with COX-deficient Leigh syndrome.
|
14564068 |
2001 |
rs782024654
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1 gene mutations in Polish patients with COX-deficient Leigh syndrome.
|
14564068 |
2001 |
rs782033035
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
SURF1 gene mutations in Polish patients with COX-deficient Leigh syndrome.
|
14564068 |
2001 |
rs121918658
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.
|
10746561 |
2000 |
rs28933402
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.
|
10746561 |
2000 |
rs398122806
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.
|
10746561 |
2000 |
rs782024654
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.
|
10746561 |
2000 |
rs782033035
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
Missense mutations in SURF1 associated with deficient cytochrome c oxidase assembly in Leigh syndrome patients.
|
10746561 |
2000 |