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Novel splice site mutations and a large deletion in three patients with the cblF inborn error of vitamin B12 metabolism

✍ Scribed by Isabelle R. Miousse; David Watkins; David S. Rosenblatt


Book ID
116989277
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
219 KB
Volume
102
Category
Article
ISSN
1096-7192

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