Cite
HARVARD Citation
Ali, G. et al. (2021). Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome. BioMed research international. p. . [Online].
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Ali, G. et al. (2021). Identification of a Novel Homozygous Missense (c.443A>T:p.N148I) Mutation in BBS2 in a Kashmiri Family with Bardet-Biedl Syndrome. BioMed research international. p. . [Online].