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- NP884292.RAcwc9M129NsuYMj-oQZUoYlg9SRSnAVYj4OpBMl5nrpM130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP884292.RAcwc9M129NsuYMj-oQZUoYlg9SRSnAVYj4OpBMl5nrpM130_provenance.
- NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568185.RASdnR2XtX5g2XL4NRIjozVuwn3ZNt-c32hgTAktxqWYA130_provenance.
- assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322901.RAhDrIIfcANDjF8KsJfzHSXa-I1rM7joRISI_w4UIDxNs130_provenance.
- NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.