Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function.
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Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function.
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name
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@en
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@nl
type
label
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@en
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@nl
prefLabel
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@en
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@nl
P2093
P2860
P50
P1433
P1476
Biallelic CHP1 mutation causes ...... ia by impairing NHE1 function.
@en
P2093
Brunhilde Wirth
Christian Pichlo
Eva Janzen
Heiko Löhr
Janine Milbradt
Laura Torres-Benito
Marie Coutelier
Markus Riessland
Mert Karakaya
Natalia Mendoza-Ferreira
P2860
P356
10.1212/NXG.0000000000000209
P577
2018-01-19T00:00:00Z