Overview of included studies for PxMD-PDHA1:
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carrying
Country
Study Study design N cases Ethnicities Sex
(% )
Mean AAO (+/- SD) Reported mutations
Dong, 2019 Mutational screen 1 A 100% 3 p.Ser388Terfs: n.a.
Asencio, 2016 Case report/Case series 1 n.a. 100% 0 p.Gly278Arg : n.a.
Castiglioni, 2015 Case report/Case series 1 C 0% 0 p.Leu216Ser: het
van Dongen, 2015 Case report/Case series 8 C 63% 2(+/-3) p.Val171Met: het
p.Pro316Leu: het
p.Met210Val: n.a.
p.Arg378Cys: n.a.
p.Lys387*: het
p.Arg263Gly: n.a.
p.Ile87Met: n.a.
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Giribaldi, 2012 Case report/Case series 1 n.a. 100% 3 p.Ala349Thr: n.a.
Magner, 2011 Case report/Case series 2 C 100% 4(+/-5) p.Thr286Ile: n.a.
p.Phe123Leu: n.a.
Quintana, 2010 Mutational screen 4 n.a. 25% n.a. p.His113Asn: het
p.Ala198Thr: het
p.Arg302Cys: het
c.(1143+1_1144-1)_(1167+1_1168-1)dup: n.a.
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Barnerias, 2010 Case report/Case series 8 n.a. 75% 0(+/-1) p.Tyr243Ser: n.a.
p.Ser312del: het
p.Arg127Gln: het
c.759+26G>A: n.a.
p.Gly185Gly: n.a.
p.Arg235Gly: n.a.
p.Arg263Gly: n.a.
p.Arg72Cys: n.a.
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Bachmann-Gagescu, 2009 Case report/Case series 1 n.a. 100% 7 p.Arg263Gly: n.a.
Ostergaard, 2009 Other/Mixed 3 n.a. 67% 3(+/-0) p.Met153Val: n.a.
p.Gly278Arg : n.a.
p.Glu206Lys: het