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UnknownSURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease.
Not available
S-EPMC3888171 | biostudies-literature
UnknownReccurrent F8 Intronic Deletion Found in Mild Hemophilia A Causes Alu Exonization.
Not available
S-EPMC5985402 | biostudies-literature
UnknownFAK-MAPK-dependent adhesion disassembly downstream of L1 contributes to semaphorin3A-induced collapse.
Not available
S-EPMC2426724 | biostudies-literature
UnknownKinetic properties of mutant deoxyguanosine kinase in a case of reversible hepatic mtDNA depletion.
Not available
S-EPMC1798436 | biostudies-literature
UnknownFAK-MAPK-dependent adhesion disassembly downstream of L1 contributes to semaphorin3A-induced collapse.
Not available
S-EPMC10183813 | biostudies-literature
UnknownA balance of noncanonical Semaphorin signaling from the cerebrospinal fluid regulates apical cell dynamics during corticogenesis.
Not available
S-EPMC9674300 | biostudies-literature
UnknownSlitC-PlexinA1 mediates iterative inhibition for orderly passage of spinal commissural axons through the floor plate.
Not available
S-EPMC7775108 | biostudies-literature
UnknownA locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15.
Not available
S-EPMC1287937 | biostudies-literature
UnknownOne-Year Effectiveness of Upadacitinib in Perianal Crohn's Disease: A Real-World GETAID Study.
Not available
S-EPMC13309209 | biostudies-literature
UnknownMolecular and functional analysis of two new MTTP gene mutations in an atypical case of abetalipoproteinemia.
Not available
S-EPMC3276478 | biostudies-literature
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