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A human gene homologous to the formin gene residing at the murine limb deformity locus: chromosomal location and RFLPs.

The murine limb deformity (ld) locus resides on mouse chromosome 2 and gives rise to a recessively inherited, characteristic limb deformity/renal aplasia phenotype. In this locus in the mouse, a gene, termed the "formin" gene, has been identified which encodes an array of differentially pr...

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Autors principals: Maas, R L, Jepeal, L I, Elfering, S L, Holcombe, R F, Morton, C C, Eddy, R L, Byers, M G, Shows, T B, Leder, P
Format: Artigo
Idioma:Inglês
Publicat: 1991
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682958/
https://ncbi.nlm.nih.gov/pubmed/1673046
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