SCOPUS 정보 검색 플랫폼

Brain and Development

Volumn 25, Issue 3, 2003, Pages 155-158

The floppy weak infant revisited

(1) Johnston, Heather M a

a SYDNEY CHILDREN'S HOSPITAL (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DISEASE COURSE; EDITORIAL; FUKUYAMA DYSTROPHY; GLYCOGEN STORAGE DISEASE; HUMAN; INFANT; INFANTILE HYPOTONIA; LABORATORY TEST; LAMININ ALPHA 2 CHAIN DEFICIENCY; MITOCHONDRIAL MYOPATHY; MUSCLE EYE BRAIN DISEASE; MUSCULAR DYSTROPHY; MYASTHENIA GRAVIS; MYOTONIC DYSTROPHY; NERVE BIOPSY; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PERIPHERAL NEUROPATHY; PHENOTYPE; PROTEIN DEFICIENCY; SPINAL CORD DISEASE; SPINAL MUSCULAR ATROPHY; WALKER WARBURG SYNDROME;

EID: 0037385026 PISSN: 03877604 EISSN: None Source Type: Journal
DOI: 10.1016/S0387-7604(02)00168-7 Document Type: Editorial

Times cited : (24)

References (8)

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2
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4
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- Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.