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Q33818078-E555F641-5F50-4EDA-B4CD-1479881FC5A1
Q33818078-E555F641-5F50-4EDA-B4CD-1479881FC5A1
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Statement
http://www.wikidata.org/entity/statement/Q33818078-E555F641-5F50-4EDA-B4CD-1479881FC5A1
Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family: A case report
P2860
Q33818078-E555F641-5F50-4EDA-B4CD-1479881FC5A1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33818078-E555F641-5F50-4EDA-B4CD-1479881FC5A1
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wasDerivedFrom
100217bf5b4c2d6289ec3da26cd7d1714cd25984
P2860
Homozygosity haplotype allows a genomewide search for the autosomal segments shared among patients.