A homozygous mutation in a consanguineous family consolidates the role of ALDH1A3 in autosomal recessive microphthalmia
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Z. Tümer | K. Grønskov | H. Jensen | L. Roos | M. Fang | C. Dali | N. Christoffersen | B. Wu | J. Zhang | R. Xu | P. Harris | X. Xu | K. Grønskov | Pernille Harris | Mingyan Fang | Hanne Jensen