Pages that link to "Q57624181"

The following pages link to Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A (Q57624181):

Displaying 10 items.

• The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease (Q28211137) (← links)
• Edg-2 in myelin-forming cells: isoforms, genomic mapping, and exclusion in Charcot-Marie-Tooth disease (Q28583631) (← links)
• Cell expression of GDAP1 in the nervous system and pathogenesis of Charcot-Marie-Tooth type 4A disease (Q28854289) (← links)
• Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3. (Q31882183) (← links)
• Dejerine-Sottas disease and hereditary demyelinating polyneuropathy of infancy (Q34981298) (← links)
• Inherited neuropathies (Q34997859) (← links)
• A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy (Q35909672) (← links)
• The autosomal recessive form of CMT disease linked to 5q31-q33. (Q39035900) (← links)
• Molecular cytogenetic analysis of consistent abnormalities at 8q12-q22 in breast cancer. (Q46171268) (← links)
• The autosomal recessive form of CMT disease linked to 5q31-q33. (Q46740562) (← links)