Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)

Richard A. Spritz; Seung Taek Lee; Kazuyoshi Fukai; Karen Brondum-Nielsen; David Chitayat; Mark H. Lipson; Maria A. Musarella; Ada Rosenmann; Richard G. Weleber

doi:10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)

Richard A. Spritz, Seung Taek Lee, Kazuyoshi Fukai, Karen Brondum-Nielsen, David Chitayat, Mark H. Lipson, Maria A. Musarella, Ada Rosenmann, Richard G. Weleber

Research output: Contribution to journal › Article › peer-review

20 Citations (Scopus)

Original language	English
Pages (from-to)	175-177
Number of pages	3
Journal	Human mutation
Volume	10
Issue number	2
DOIs	https://doi.org/10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X
Publication status	Published - 1997

All Science Journal Classification (ASJC) codes

Genetics
Genetics(clinical)

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10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X

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title = "Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)",

author = "Spritz, {Richard A.} and Lee, {Seung Taek} and Kazuyoshi Fukai and Karen Brondum-Nielsen and David Chitayat and Lipson, {Mark H.} and Musarella, {Maria A.} and Ada Rosenmann and Weleber, {Richard G.}",

year = "1997",

doi = "10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X",

language = "English",

volume = "10",

pages = "175--177",

journal = "Human mutation",

issn = "1059-7794",

publisher = "Wiley-Liss Inc.",

number = "2",

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TY - JOUR

T1 - Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)

AU - Spritz, Richard A.

AU - Lee, Seung Taek

AU - Fukai, Kazuyoshi

AU - Brondum-Nielsen, Karen

AU - Chitayat, David

AU - Lipson, Mark H.

AU - Musarella, Maria A.

AU - Rosenmann, Ada

AU - Weleber, Richard G.

PY - 1997

Y1 - 1997

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U2 - 10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X

DO - 10.1002/(SICI)1098-1004(1997)10:2<175::AID-HUMU12>3.0.CO;2-X

M3 - Article

C2 - 9259203

AN - SCOPUS:0030790959

SN - 1059-7794

VL - 10

SP - 175

EP - 177

JO - Human mutation

JF - Human mutation

IS - 2

ER -

Novel mutations of the P gene in type II oculocutaneous albinism (OCA2)

All Science Journal Classification (ASJC) codes

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