Molecular basis of variant pseudo-Hurler polydystrophy (mucolipidosis IIIC)

Journal of Clinical Investigation

Volumn 105, Issue 5, 2000, Pages 673-681

  Raas Rothschild, Annick ^a,b   Cormier Daire, Valerie ^b   Bao, Ming ^c   Genin, Emmanuelle ^d   Salomon, Remi ^b   Brewer, Kevin ^c   Zeigler, Marsha ^a   Mandel, Hanna ^e   Toth, Steve ^f   Roe, Bruce ^f   Munnich, Arnold ^b   Canfield, William M ^c,g  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b HÔPITAL NECKER ENFANTS MALADES   (France)

^c UNIVERSITY OF OKLAHOMA COLLEGE OF MEDICINE   (United States)

^d INSERM   (France)

^e RAMBAM MEDICAL CENTER   (Israel)

^f UNIVERSITY OF OKLAHOMA   (United States)

^g UNIVERSITY OF OKLAHOMA HEALTH SCIENCES CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 16P; CHROMOSOME MAP; DISEASE ASSOCIATION; ENZYME ACTIVITY; FRAMESHIFT MUTATION; HUMAN; MOLECULAR CLONING; MUCOLIPIDOSIS TYPE 3; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

EID: 19244386351     PISSN: 00219738     EISSN: None     Source Type: Journal    
DOI: 10.1172/JCI5826     Document Type: Article

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