Corrigendum to "Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737)" [Mol. Genet. Metab. 77 (2002) 252-256] (DOI:10.1016/S1096-7192(02)00141-5);Four novel mutations associated with autosomal recessive inclusion body myopathy (MIM: 600737)

Molecular Genetics and Metabolism

Volumn 77, Issue 3, 2002, Pages 252-256

  Darvish, D ^a   Vahedifar, P ^a   Huo, Y ^a  

^a IBM RESEARCH   (United States)

Author keywords

IBM2; N Acetylmannosamine (ManNAc); Neuraminate; Neuraminic acid; Nonaka's myopathy; Recessive hereditary inclusion body myopathy (rHIBM); Sialic acid; Sialic acid synthesis pathway; UDP N acetylglucosamine 2 epimerase (GNE) N acetylmannosamine kinase (MNK)

Indexed keywords

EPIMERASE; N ACETYLMANNOSAMINE KINASE; PHOSPHOTRANSFERASE; UNCLASSIFIED DRUG; URIDINE DIPHOSPHATE N ACETYLGLUCOSAMINE 2 EPIMERASE; N ACYLMANNOSAMINE KINASE; N-ACYLMANNOSAMINE KINASE; UDP ACETYLGLUCOSAMINE 2 EPIMERASE; UDP ACETYLGLUCOSAMINE-2-EPIMERASE;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL VACUOLE; CODON; CONTROLLED STUDY; ETHNOLOGY; GENE MUTATION; GENETIC ASSOCIATION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; INCLUSION BODY MYOSITIS; IRAN; JEW; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; NEGATIVE FEEDBACK; POLYMORPHIC LOCUS; PRIORITY JOURNAL; PROTEIN DOMAIN; REGULATORY MECHANISM; DNA SEQUENCE; FEMALE; GENETICS; MALE; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; RECESSIVE GENE;

IRANIA;

ADULT; CARBOHYDRATE EPIMERASES; DNA MUTATIONAL ANALYSIS; FEMALE; GENES, RECESSIVE; HUMANS; MALE; MUTATION; MYOSITIS, INCLUSION BODY; PEDIGREE; PHOSPHOTRANSFERASES (ALCOHOL GROUP ACCEPTOR); SEQUENCE ANALYSIS, DNA;

EID: 0036431973     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2006.05.006     Document Type: Erratum

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