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UnknownBi-allelic loss of ERGIC1 causes relatively mild arthrogryposis.
Not available
S-EPMC8453841 | biostudies-literature
UnknownDNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defects.
Not available
S-EPMC2662904 | biostudies-literature
UnknownMutations in ZMYND10, a gene essential for proper axonemal assembly of inner and outer dynein arms in humans and flies, cause primary ciliary dyskinesia.
Not available
S-EPMC3738835 | biostudies-literature
UnknownGenome scan meta-analysis of schizophrenia and bipolar disorder, part II: Schizophrenia.
Not available
S-EPMC1180588 | biostudies-literature
UnknownX-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3.
Not available
S-EPMC5309803 | biostudies-literature
UnknownGenome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.
Not available
S-EPMC1180589 | biostudies-literature
UnknownEchocardiographic evidence for valvular toxicity of benfluorex: a double-blind randomised trial in patients with type 2 diabetes mellitus.
Not available
S-EPMC3378581 | biostudies-literature
UnknownTitin-related familial dilated cardiomyopathy: factors associated with disease onset.
Not available
S-EPMC12718689 | biostudies-literature
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