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Matches in Nanopublications for { ?s ?p "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP1232253.RAaxd_qMV163H07IAIyNZPC-3uWBFfAqYhkGnz35uO0rI130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232253.RAaxd_qMV163H07IAIyNZPC-3uWBFfAqYhkGnz35uO0rI130_provenance.
• NP1232255.RAXhwr0VDZju4jLtDW9ykPaSsDujsHPQxFgMKvLPSAM5o130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232255.RAXhwr0VDZju4jLtDW9ykPaSsDujsHPQxFgMKvLPSAM5o130_provenance.
• NP1232258.RAc0dzVkm34pk-8cH6btU7rMBPzYoBWDt7cIbknjbh6eE130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232258.RAc0dzVkm34pk-8cH6btU7rMBPzYoBWDt7cIbknjbh6eE130_provenance.
• NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232256.RAqcLyG77bKuejDFZuDE-ZNCf-GWpDmpN7qI0hy8t2Bf0130_provenance.
• NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232252.RAE_7imUl9lNSSGX-3SD2NoX3U7XWW71aRtiaycy1sJZA130_provenance.
• NP1232254.RAIv_RRpviHp_YsaQONkcRN9xjDFoLbj-kf3Fk3Ga43hk130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232254.RAIv_RRpviHp_YsaQONkcRN9xjDFoLbj-kf3Fk3Ga43hk130_provenance.
• NP1232257.RA6BCh2rcPXpLYO_7knsECNUTGefVzpvypeuw64gY6ydY130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232257.RA6BCh2rcPXpLYO_7knsECNUTGefVzpvypeuw64gY6ydY130_provenance.
• NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_assertion description "[We aimed to establish the importance of HINT1 mutations as the cause of hereditary neuropathy and particularly hereditary motor neuropathy/axonal Charcot-Marie-Tooth (HMN/CMT2) among Czech patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1232259.RA4eHoUDbRny0o1DgNdSGgSTATCPyH5ZCpyqdtNHd4G90130_provenance.