Condition: Gait abnormality
rs1557055405
in
ABCD1
gene and
Gait abnormality
PMID 9452087
1998 First missense mutation (W679R) in exon 10 of the adrenoleukodystrophy gene in siblings with adrenomyeloneuropathy.
rs778361520
in
ADGRB2
gene and
Gait abnormality
PMID 28891236
2017 A disease-associated mutation in the adhesion GPCR BAI2 (ADGRB2) increases receptor signaling activity.
rs387906905
in
TRPV4
gene and
Gait abnormality
PMID 21288981
2011 TRPV4 mutations and cytotoxic hypercalcemia in axonal Charcot-Marie-Tooth neuropathies.