The genomic structure, chromosomal localization, and analysis of SIL as a candidate gene for holoprosencephaly

Author:

Karkera J.D.,Izraeli S.,Roessler E.,Dutra A.,Kirsch I.,Muenke M.

Publisher

S. Karger AG

Subject

Genetics(clinical),Genetics,Molecular Biology

Cited by 19 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. STIL: a multi-function protein required for dopaminergic neural proliferation, protection, and regeneration;Cell Death Discovery;2019-04-25

2. Recent advances in understanding inheritance of holoprosencephaly;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-05-22

3. Holoprosencephaly in the genomics era;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-05-17

4. Homozygous STIL Mutation Causes Holoprosencephaly and Microcephaly in Two Siblings;PLOS ONE;2015-02-06

5. STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly;Human Genetics;2014-09-14

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