COWCHOCK SYNDROME

Known as: COWCK, CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 4, Charcot-Marie-Tooth disease with deafness and mental retardation 
 
National Institutes of Health

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2016
2016
AIFM1 is a gene located on the X chromosome, coding for AIF (Apoptosis-Inducing Factor), a mitochondrial flavoprotein involved in… (More)
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2012
2012
Cowchock syndrome (CMTX4) is a slowly progressive X-linked recessive disorder with axonal neuropathy, deafness, and cognitive… (More)
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Review
2010
Review
2010
Dear Sirs, Charcot-Marie-Tooth (CMT) disease encompasses a clinically and genetically heterogeneous group of inherited peripheral… (More)
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