杂合 TGFBR2 突变在马凡氏综合征中的应用.
Mesh : Amino Acid Sequence Chromosomes, Human, Pair 3 Female Humans Male Marfan Syndrome / genetics Molecular Sequence Data Mutation Pedigree Protein Serine-Threonine Kinases Receptor, Transforming Growth Factor-beta Type II Receptors, Transforming Growth Factor beta / genetics Signal Transduction / genetics
来 源:
DOI:10.1038/ng1392
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