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. Author manuscript; available in PMC: 2018 May 1.
Published in final edited form as: Neuromuscul Disord. 2017 Feb 6;27(5):439–446. doi: 10.1016/j.nmd.2017.02.002

Figure 1. Identification of familial relationships within family #3042 of the NIGMS Cell Collection using the D8S1179 microsatellite marker.

Figure 1

(A) Pedigree analysis of family #3042. GM23686 was diagnosed with type I SMA. (B) Electrophoretograms showing the D8S1179 alleles for GM23686, GM23687 and GM23688.