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Volumn 18, Issue 2, 2011, Pages 207-217

EFNS guidelines for the molecular diagnosis of neurogenetic disorders: Motoneuron, peripheral nerve and muscle disorders

(18)  Burgunder, J M a   Schols L b   Baets, J c,d,e   Andersen, P f   Gasser, T g   Szolnoki, Z h   Fontaine, B i   Van Broeckhoven, C d,e   Di Donato, S j   De Jonghe, P c,d,e   Lynch, T k   Mariotti, C j   Spinazzola, A j   Tabrizi, S J l   Tallaksen, C m   Zeviani, M j   Harbo, H F m   Finsterer, J n  


Author keywords

Amyotrophic lateral sclerosis; EFNS task force; Molecular diagnosis; Myopathy; Neurogenetics; Polyneuropathy; Spinal muscular atrophy

Indexed keywords

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CLINICAL FEATURE; CLINICAL PRACTICE; DUCHENNE MUSCULAR DYSTROPHY; FAMILIAL DISEASE; GENETIC DISORDER; GENETIC SCREENING; HEREDITARY MOTOR SENSORY NEUROPATHY; INFORMATION PROCESSING; KENNEDY DISEASE; MEDICAL DECISION MAKING; MOLECULAR DIAGNOSIS; MYOPATHY; MYOTONIC DYSTROPHY; NEUROLOGIC DISEASE; NEUROPATHY; PHENOTYPE; PRACTICE GUIDELINE; PRIORITY JOURNAL; SPINAL MUSCULAR ATROPHY;

EID: 78751491533     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1111/j.1468-1331.2010.03069.x     Document Type: Article
Times cited : (38)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.