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Progressive hearing loss associated with a unique cervical node due to a homozygous SLC29A3 mutation: A very mild phenotype

✍ Scribed by Laurence Jonard; Vincent Couloigner; Sébastien Pierrot; Malek Louha; Souad Gherbi; Françoise Denoyelle; Sandrine Marlin


Book ID
116433413
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
439 KB
Volume
55
Category
Article
ISSN
1769-7212

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