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Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss

✍ Scribed by Rasheeda Bashir; Amara Fatima; Sadaf Naz


Book ID
116433443
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
363 KB
Volume
55
Category
Article
ISSN
1769-7212

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