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2026
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2024
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2020
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Comprehensive analysis of two hotspot codons in the TUBB4B gene and associated phenotypes.
Not available
S-EPMC11078972
|
biostudies-literature
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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations.
Not available
S-EPMC7536580
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biostudies-literature
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Loss-of-function variants in the CAPN1 activator CD99L2 cause X-linked spastic ataxia.
Not available
S-EPMC12910011
|
biostudies-literature
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