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F1000RESEARCH.12102.1
F1000RESEARCH.12102.1
http://dx.doi.org/10.12688/F1000RESEARCH.12102.1
Whole exome sequencing identifies a novel homozygous frameshift mutation in the ASPM gene, which causes microcephaly 5, primary, autosomal recessive.
P356
Q47708439-DD11D749-8F3F-406C-8F34-172EB1C3DF62
P356
F1000RESEARCH.12102.1
http://dx.doi.org/10.12688/F1000RESEARCH.12102.1