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Mild clinical phenotype in a 12-year-old boy with partial merosin deficiency and central and peripheral nervous system abnormalities

✍ Scribed by Marina Mora; Isabella Moroni; Graziella Uziel; Claudia Di Blasi; Rita Barresi; Laura Farina; Lucia Morandi


Book ID
116168630
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
302 KB
Volume
6
Category
Article
ISSN
0960-8966

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