Spectrum of Δ7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (Human Molecular Genetics (2000) vol.9 (1385-1391))

H. Yu; M. H. Lee; L. Starch; E. R. Elias; M. Irons; G. Salen; S. B. Patel; G. S. Tint

Spectrum of Δ7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (Human Molecular Genetics (2000) vol.9 (1385-1391))

H. Yu, M. H. Lee, L. Starch, E. R. Elias, M. Irons, G. Salen, S. B. Patel, G. S. Tint

Research output: Contribution to journal › Comment/debate › peer-review

Original language	English (US)
Pages (from-to)	1903
Number of pages	1
Journal	Human molecular genetics
Volume	9
Issue number	12
State	Published - 2000
Externally published	Yes

ASJC Scopus subject areas

Molecular Biology
Genetics
Genetics(clinical)

Cite this

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title = "Spectrum of Δ7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (Human Molecular Genetics (2000) vol.9 (1385-1391))",

author = "H. Yu and Lee, {M. H.} and L. Starch and Elias, {E. R.} and M. Irons and G. Salen and Patel, {S. B.} and Tint, {G. S.}",

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journal = "Human Molecular Genetics",

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T1 - Spectrum of Δ7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (Human Molecular Genetics (2000) vol.9 (1385-1391))

AU - Yu, H.

AU - Lee, M. H.

AU - Starch, L.

AU - Elias, E. R.

AU - Irons, M.

AU - Salen, G.

AU - Patel, S. B.

AU - Tint, G. S.

PY - 2000

Y1 - 2000

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M3 - Comment/debate

AN - SCOPUS:0033861699

SN - 0964-6906

VL - 9

SP - 1903

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 12

ER -

Spectrum of Δ7-dehydrocholesterol reductase mutations in patients with the Smith-Lemli-Opitz (RSH) syndrome (Human Molecular Genetics (2000) vol.9 (1385-1391))

ASJC Scopus subject areas

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